Canonical Allele Identifier: CA3871609
Community Standard Title: NM_001374736.1(DST):c.1779-261C>T
Gene: DST HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.56642764G>A , CM000668.2:g.56642764G>A GRCh38
NC_000006.11:g.56507562G>A , CM000668.1:g.56507562G>A GRCh37
NC_000006.10:g.56615521G>A NCBI36
NG_029322.1:g.5133C>T
NG_029322.2:g.316865C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001374736.1:c.1779-261C>T MANE Select NP_001361665.1:n.1779-261C>T
ENST00000680361.1:c.1779-261C>T MANE Select ENSP00000505098.1:n.1779-261C>T
NM_001723.7:c.25C>T MANE Plus Clinical NP_001714.1:p.Arg9Cys
ENST00000370765.11:c.25C>T MANE Plus Clinical ENSP00000359801.6:p.Arg9Cys
NM_001144769.2:c.1680-261C>T NP_001138241.1:n.1680-261C>T
NM_001144769.5:c.1680-261C>T NP_001138241.1:n.1680-261C>T
NM_001144770.1:c.1266-261C>T NP_001138242.1:n.1266-261C>T
NM_001144770.2:c.1266-261C>T NP_001138242.1:n.1266-261C>T
NM_001374722.1:c.1779-261C>T NP_001361651.1:n.1779-261C>T
NM_001374729.1:c.1146-261C>T NP_001361658.1:n.1146-261C>T
NM_001374730.1:c.1146-261C>T NP_001361659.1:n.1146-261C>T
NM_001374734.1:c.1806-261C>T NP_001361663.1:n.1806-261C>T
NM_001386100.1:c.1146-261C>T NP_001373029.1:n.1146-261C>T
NM_001723.5:c.25C>T NP_001714.1:p.Arg9Cys
NM_001723.6:c.25C>T NP_001714.1:p.Arg9Cys
NM_015548.4:c.25C>T NP_056363.2:p.Arg9Cys
NM_015548.5:c.25C>T NP_056363.2:p.Arg9Cys
NM_183380.3:c.1146-261C>T NP_899236.1:n.1146-261C>T
NM_183380.4:c.1146-261C>T NP_899236.1:n.1146-261C>T
ENST00000244364.10:c.25C>T ENSP00000244364.6:p.Arg9Cys
ENST00000312431.10:c.1266-261C>T ENSP00000307959.7:n.1266-261C>T
ENST00000361203.7:c.1146-261C>T ENSP00000354508.3:n.1146-261C>T
ENST00000370754.9:c.1680-261C>T ENSP00000359790.6:n.1680-261C>T
ENST00000370765.10:c.25C>T ENSP00000359801.6:p.Arg9Cys
ENST00000370788.6:c.1146-261C>T ENSP00000359824.2:n.1146-261C>T
ENST00000421834.6:c.1146-261C>T ENSP00000400883.3:n.1146-261C>T
ENST00000421834.7:c.1146-261C>T ENSP00000400883.3:n.1146-261C>T
ENST00000439203.5:c.25C>T ENSP00000404924.1:p.Arg9Cys
ENST00000449297.6:c.1680-261C>T ENSP00000393082.2:n.1680-261C>T
ENST00000449297.7:c.1680-261C>T ENSP00000393082.3:n.1680-261C>T
ENST00000518828.1:n.126C>T
ENST00000518935.5:c.25C>T ENSP00000431003.1:p.Arg9Cys
ENST00000520645.5:c.1266-261C>T ENSP00000431030.1:n.1266-261C>T
ENST00000520645.6:c.1266-261C>T ENSP00000431030.2:n.1266-261C>T
ENST00000521104.1:n.1648-261C>T
ENST00000523967.5:n.1376-261C>T
ENST00000652573.1:c.1494-261C>T ENSP00000498983.1:n.1494-261C>T
XM_005249310.2:c.1779-261C>T XP_005249367.1:n.1779-261C>T
XM_005249310.4:c.1779-261C>T XP_005249367.1:n.1779-261C>T
XM_005249315.2:c.1680-261C>T XP_005249372.1:n.1680-261C>T
XM_005249315.3:c.1680-261C>T XP_005249372.1:n.1680-261C>T
XM_005249316.1:c.1494-261C>T XP_005249373.1:n.1494-261C>T
XM_005249316.3:c.1494-261C>T XP_005249373.1:n.1494-261C>T
XM_005249318.1:c.1365-261C>T XP_005249375.1:n.1365-261C>T
XM_005249318.2:c.1365-261C>T XP_005249375.1:n.1365-261C>T
XM_005249319.1:c.1266-261C>T XP_005249376.1:n.1266-261C>T
XM_005249319.2:c.1266-261C>T XP_005249376.1:n.1266-261C>T
XM_005249320.3:c.1245-261C>T XP_005249377.1:n.1245-261C>T
XM_005249320.4:c.1245-261C>T XP_005249377.1:n.1245-261C>T
XM_005249322.3:c.1224-261C>T XP_005249379.1:n.1224-261C>T
XM_005249322.5:c.1224-261C>T XP_005249379.1:n.1224-261C>T
XM_005249323.2:c.1146-261C>T XP_005249380.1:n.1146-261C>T
XM_005249323.4:c.1146-261C>T XP_005249380.1:n.1146-261C>T
XM_005249324.1:c.25C>T XP_005249381.1:p.Arg9Cys
XM_005249324.3:c.25C>T XP_005249381.1:p.Arg9Cys
XM_011514824.1:c.1707-261C>T XP_011513126.1:n.1707-261C>T
XM_011514824.2:c.1707-261C>T XP_011513126.1:n.1707-261C>T
XM_011514825.1:c.1707-261C>T XP_011513127.1:n.1707-261C>T
XM_011514825.3:c.1707-261C>T XP_011513127.1:n.1707-261C>T
XM_011514826.1:c.1146-261C>T XP_011513128.1:n.1146-261C>T
XM_011514826.3:c.1146-261C>T XP_011513128.1:n.1146-261C>T
XM_017011205.1:c.1806-261C>T XP_016866694.1:n.1806-261C>T
XM_017011206.1:c.1806-261C>T XP_016866695.1:n.1806-261C>T
XM_017011207.1:c.1743-261C>T XP_016866696.1:n.1743-261C>T
XM_017011208.1:c.1806-261C>T XP_016866697.1:n.1806-261C>T
XM_017011209.1:c.1806-261C>T XP_016866698.1:n.1806-261C>T
XM_017011210.1:c.1806-261C>T XP_016866699.1:n.1806-261C>T
XM_017011211.2:c.1806-261C>T XP_016866700.1:n.1806-261C>T
XM_017011212.1:c.1806-261C>T XP_016866701.1:n.1806-261C>T
XM_017011213.1:c.1806-261C>T XP_016866702.1:n.1806-261C>T
XM_017011214.2:c.1806-261C>T XP_016866703.1:n.1806-261C>T
XM_017011215.2:c.1806-261C>T XP_016866704.1:n.1806-261C>T
XM_017011216.2:c.1806-261C>T XP_016866705.1:n.1806-261C>T
XM_017011217.1:c.1182-261C>T XP_016866706.1:n.1182-261C>T
XM_017011219.1:c.1806-261C>T XP_016866708.1:n.1806-261C>T
XM_017011220.1:c.1680-261C>T XP_016866709.1:n.1680-261C>T
XM_017011221.1:c.1806-261C>T XP_016866710.1:n.1806-261C>T
XM_017011222.2:c.1494-261C>T XP_016866711.1:n.1494-261C>T
XM_017011223.1:c.1806-261C>T XP_016866712.1:n.1806-261C>T
XM_017011224.2:c.1146-261C>T XP_016866713.1:n.1146-261C>T
XM_017011225.2:c.1806-261C>T XP_016866714.1:n.1806-261C>T
XM_024446530.1:c.1125-261C>T XP_024302298.1:n.1125-261C>T
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