Canonical Allele Identifier: CA1630147875
Community Standard Title: NM_001374736.1(DST):c.14741G= (p.Arg4914=)
Gene: DST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.56555740C= , CM000668.2:g.56555740C= GRCh38
NC_000006.11:g.56420538C= , CM000668.1:g.56420538C= GRCh37
NC_000006.10:g.56528497C= NCBI36
NG_029322.1:g.92157G=
NG_029322.2:g.403889G=

Transcript Alleles

HGVS Amino-acid Change
NM_001374736.1:c.14741G= MANE Select NP_001361665.1:p.Arg4914=
ENST00000680361.1:c.14741G= MANE Select ENSP00000505098.1:p.Arg4914=
NM_001144769.2:c.8384G= NP_001138241.1:p.Arg2795=
NM_001144769.5:c.8384G= NP_001138241.1:p.Arg2795=
NM_001144770.1:c.7970G= NP_001138242.1:p.Arg2657=
NM_001144770.2:c.7970G= NP_001138242.1:p.Arg2657=
NM_001374722.1:c.14741G= NP_001361651.1:p.Arg4914=
NM_001374729.1:c.14108G= NP_001361658.1:p.Arg4703=
NM_001374730.1:c.7850G= NP_001361659.1:p.Arg2617=
NM_001374734.1:c.14768G= NP_001361663.1:p.Arg4923=
NM_001386100.1:c.7850G= NP_001373029.1:p.Arg2617=
NM_015548.4:c.6872G= NP_056363.2:p.Arg2291=
NM_015548.5:c.6872G= NP_056363.2:p.Arg2291=
NM_183380.3:c.7850G= NP_899236.1:p.Arg2617=
NM_183380.4:c.7850G= NP_899236.1:p.Arg2617=
ENST00000244364.10:c.6872G= ENSP00000244364.6:p.Arg2291=
ENST00000312431.10:c.7970G= ENSP00000307959.7:p.Arg2657=
ENST00000361203.7:c.14108G= ENSP00000354508.3:p.Arg4703=
ENST00000370754.9:c.8384G= ENSP00000359790.6:p.Arg2795=
ENST00000370788.6:c.7850G= ENSP00000359824.2:p.Arg2617=
ENST00000421834.6:c.7850G= ENSP00000400883.3:p.Arg2617=
ENST00000421834.7:c.7850G= ENSP00000400883.3:p.Arg2617=
ENST00000449297.7:c.8384G= ENSP00000393082.3:p.Arg2795=
ENST00000520144.1:n.450G=
ENST00000520144.2:n.712G=
ENST00000520645.6:c.7970G= ENSP00000431030.2:p.Arg2657=
XM_005249310.2:c.14741G= XP_005249367.1:p.Arg4914=
XM_005249310.4:c.14741G= XP_005249367.1:p.Arg4914=
XM_005249315.2:c.14642G= XP_005249372.1:p.Arg4881=
XM_005249315.3:c.14642G= XP_005249372.1:p.Arg4881=
XM_005249316.1:c.14456G= XP_005249373.1:p.Arg4819=
XM_005249316.3:c.14456G= XP_005249373.1:p.Arg4819=
XM_005249318.1:c.14327G= XP_005249375.1:p.Arg4776=
XM_005249318.2:c.14327G= XP_005249375.1:p.Arg4776=
XM_005249319.1:c.14228G= XP_005249376.1:p.Arg4743=
XM_005249319.2:c.14228G= XP_005249376.1:p.Arg4743=
XM_005249320.3:c.14207G= XP_005249377.1:p.Arg4736=
XM_005249320.4:c.14207G= XP_005249377.1:p.Arg4736=
XM_005249322.3:c.14186G= XP_005249379.1:p.Arg4729=
XM_005249322.5:c.14186G= XP_005249379.1:p.Arg4729=
XM_005249323.2:c.14108G= XP_005249380.1:p.Arg4703=
XM_005249323.4:c.14108G= XP_005249380.1:p.Arg4703=
XM_005249324.1:c.13130G= XP_005249381.1:p.Arg4377=
XM_005249324.3:c.13130G= XP_005249381.1:p.Arg4377=
XM_011514824.1:c.14669G= XP_011513126.1:p.Arg4890=
XM_011514824.2:c.14669G= XP_011513126.1:p.Arg4890=
XM_011514825.1:c.8411G= XP_011513127.1:p.Arg2804=
XM_011514825.3:c.8411G= XP_011513127.1:p.Arg2804=
XM_011514826.1:c.14108G= XP_011513128.1:p.Arg4703=
XM_011514826.3:c.14108G= XP_011513128.1:p.Arg4703=
XM_017011205.1:c.14768G= XP_016866694.1:p.Arg4923=
XM_017011206.1:c.14768G= XP_016866695.1:p.Arg4923=
XM_017011207.1:c.14705G= XP_016866696.1:p.Arg4902=
XM_017011208.1:c.14768G= XP_016866697.1:p.Arg4923=
XM_017011209.1:c.14768G= XP_016866698.1:p.Arg4923=
XM_017011210.1:c.14768G= XP_016866699.1:p.Arg4923=
XM_017011211.2:c.14768G= XP_016866700.1:p.Arg4923=
XM_017011212.1:c.14534G= XP_016866701.1:p.Arg4845=
XM_017011213.1:c.14768G= XP_016866702.1:p.Arg4923=
XM_017011214.2:c.14768G= XP_016866703.1:p.Arg4923=
XM_017011215.2:c.14768G= XP_016866704.1:p.Arg4923=
XM_017011216.2:c.14768G= XP_016866705.1:p.Arg4923=
XM_017011217.1:c.14144G= XP_016866706.1:p.Arg4715=
XM_017011218.1:c.9335G= XP_016866707.1:p.Arg3112=
XM_017011219.1:c.8510G= XP_016866708.1:p.Arg2837=
XM_017011220.1:c.8384G= XP_016866709.1:p.Arg2795=
XM_017011221.1:c.8276G= XP_016866710.1:p.Arg2759=
XM_017011222.2:c.8198G= XP_016866711.1:p.Arg2733=
XM_017011223.1:c.8510G= XP_016866712.1:p.Arg2837=
XM_017011224.2:c.7850G= XP_016866713.1:p.Arg2617=
XM_024446530.1:c.14087G= XP_024302298.1:p.Arg4696=