Canonical Allele Identifier: CA364519381

Gene: DST

Linked Data

• MyVariant Identifiers: chr6:g.56420449G>A (hg19) ; chr6:g.56555651G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.56555651G>A , CM000668.2:g.56555651G>A	GRCh38
NC_000006.11:g.56420449G>A , CM000668.1:g.56420449G>A	GRCh37
NC_000006.10:g.56528408G>A	NCBI36
NG_029322.1:g.92246C>T
NG_029322.2:g.403978C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000421834.7:c.7939C>T	ENSP00000400883.3:p.Gln2647Ter
ENST00000449297.7:c.8473C>T	ENSP00000393082.3:p.Gln2825Ter
ENST00000520645.6:c.8059C>T	ENSP00000431030.2:p.Gln2687Ter
ENST00000520144.2:n.801C>T
ENST00000680361.1:c.14830C>T MANE Select	ENSP00000505098.1:p.Gln4944Ter
ENST00000244364.10:c.6961C>T	ENSP00000244364.6:p.Gln2321Ter
ENST00000312431.10:c.8059C>T	ENSP00000307959.7:p.Gln2687Ter
ENST00000361203.7:c.14197C>T	ENSP00000354508.3:p.Gln4733Ter
ENST00000370754.9:c.8473C>T	ENSP00000359790.6:p.Gln2825Ter
ENST00000370788.6:c.7939C>T	ENSP00000359824.2:p.Gln2647Ter
ENST00000421834.6:c.7939C>T	ENSP00000400883.3:p.Gln2647Ter
ENST00000520144.1:n.539C>T
NM_001144769.2:c.8473C>T	NP_001138241.1:p.Gln2825Ter
NM_001144770.1:c.8059C>T	NP_001138242.1:p.Gln2687Ter
NM_015548.4:c.6961C>T	NP_056363.2:p.Gln2321Ter
NM_183380.3:c.7939C>T	NP_899236.1:p.Gln2647Ter
XM_005249310.2:c.14830C>T	XP_005249367.1:p.Gln4944Ter
XM_005249315.2:c.14731C>T	XP_005249372.1:p.Gln4911Ter
XM_005249316.1:c.14545C>T	XP_005249373.1:p.Gln4849Ter
XM_005249318.1:c.14416C>T	XP_005249375.1:p.Gln4806Ter
XM_005249319.1:c.14317C>T	XP_005249376.1:p.Gln4773Ter
XM_005249320.3:c.14296C>T	XP_005249377.1:p.Gln4766Ter
XM_005249322.3:c.14275C>T	XP_005249379.1:p.Gln4759Ter
XM_005249323.2:c.14197C>T	XP_005249380.1:p.Gln4733Ter
XM_005249324.1:c.13219C>T	XP_005249381.1:p.Gln4407Ter
XM_011514824.1:c.14758C>T	XP_011513126.1:p.Gln4920Ter
XM_011514825.1:c.8500C>T	XP_011513127.1:p.Gln2834Ter
XM_011514826.1:c.14197C>T	XP_011513128.1:p.Gln4733Ter
XM_005249310.4:c.14830C>T	XP_005249367.1:p.Gln4944Ter
XM_005249315.3:c.14731C>T	XP_005249372.1:p.Gln4911Ter
XM_005249316.3:c.14545C>T	XP_005249373.1:p.Gln4849Ter
XM_005249318.2:c.14416C>T	XP_005249375.1:p.Gln4806Ter
XM_005249319.2:c.14317C>T	XP_005249376.1:p.Gln4773Ter
XM_005249320.4:c.14296C>T	XP_005249377.1:p.Gln4766Ter
XM_005249322.5:c.14275C>T	XP_005249379.1:p.Gln4759Ter
XM_005249323.4:c.14197C>T	XP_005249380.1:p.Gln4733Ter
XM_005249324.3:c.13219C>T	XP_005249381.1:p.Gln4407Ter
XM_011514824.2:c.14758C>T	XP_011513126.1:p.Gln4920Ter
XM_011514825.3:c.8500C>T	XP_011513127.1:p.Gln2834Ter
XM_011514826.3:c.14197C>T	XP_011513128.1:p.Gln4733Ter
XM_017011205.1:c.14857C>T	XP_016866694.1:p.Gln4953Ter
XM_017011206.1:c.14857C>T	XP_016866695.1:p.Gln4953Ter
XM_017011207.1:c.14794C>T	XP_016866696.1:p.Gln4932Ter
XM_017011208.1:c.14857C>T	XP_016866697.1:p.Gln4953Ter
XM_017011209.1:c.14857C>T	XP_016866698.1:p.Gln4953Ter
XM_017011210.1:c.14857C>T	XP_016866699.1:p.Gln4953Ter
XM_017011211.2:c.14857C>T	XP_016866700.1:p.Gln4953Ter
XM_017011212.1:c.14623C>T	XP_016866701.1:p.Gln4875Ter
XM_017011213.1:c.14857C>T	XP_016866702.1:p.Gln4953Ter
XM_017011214.2:c.14857C>T	XP_016866703.1:p.Gln4953Ter
XM_017011215.2:c.14857C>T	XP_016866704.1:p.Gln4953Ter
XM_017011216.2:c.14857C>T	XP_016866705.1:p.Gln4953Ter
XM_017011217.1:c.14233C>T	XP_016866706.1:p.Gln4745Ter
XM_017011218.1:c.9424C>T	XP_016866707.1:p.Gln3142Ter
XM_017011219.1:c.8599C>T	XP_016866708.1:p.Gln2867Ter
XM_017011220.1:c.8473C>T	XP_016866709.1:p.Gln2825Ter
XM_017011221.1:c.8365C>T	XP_016866710.1:p.Gln2789Ter
XM_017011222.2:c.8287C>T	XP_016866711.1:p.Gln2763Ter
XM_017011223.1:c.8599C>T	XP_016866712.1:p.Gln2867Ter
XM_017011224.2:c.7939C>T	XP_016866713.1:p.Gln2647Ter
XM_024446530.1:c.14176C>T	XP_024302298.1:p.Gln4726Ter
NM_001144769.5:c.8473C>T	NP_001138241.1:p.Gln2825Ter
NM_001144770.2:c.8059C>T	NP_001138242.1:p.Gln2687Ter
NM_001374722.1:c.14830C>T	NP_001361651.1:p.Gln4944Ter
NM_001374729.1:c.14197C>T	NP_001361658.1:p.Gln4733Ter
NM_001374730.1:c.7939C>T	NP_001361659.1:p.Gln2647Ter
NM_001374734.1:c.14857C>T	NP_001361663.1:p.Gln4953Ter
NM_001374736.1:c.14830C>T MANE Select	NP_001361665.1:p.Gln4944Ter
NM_015548.5:c.6961C>T	NP_056363.2:p.Gln2321Ter
NM_183380.4:c.7939C>T	NP_899236.1:p.Gln2647Ter
NM_001386100.1:c.7939C>T	NP_001373029.1:p.Gln2647Ter