Canonical Allele Identifier: CA1630144379

Gene: DST

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.56552484C= , CM000668.2:g.56552484C=	GRCh38
NC_000006.11:g.56417282C= , CM000668.1:g.56417282C=	GRCh37
NC_000006.10:g.56525241C=	NCBI36
NG_029322.1:g.95413G=
NG_029322.2:g.407145G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421834.7:c.9417G=	ENSP00000400883.3:p.Met3139=
ENST00000449297.7:c.9951G=	ENSP00000393082.3:p.Met3317=
ENST00000520645.6:c.9537G=	ENSP00000431030.2:p.Met3179=
ENST00000680361.1:c.16308G= MANE Select	ENSP00000505098.1:p.Met5436=
ENST00000244364.10:c.8439G=	ENSP00000244364.6:p.Met2813=
ENST00000312431.10:c.9537G=	ENSP00000307959.7:p.Met3179=
ENST00000361203.7:c.15675G=	ENSP00000354508.3:p.Met5225=
ENST00000370754.9:c.9951G=	ENSP00000359790.6:p.Met3317=
ENST00000370788.6:c.9417G=	ENSP00000359824.2:p.Met3139=
ENST00000421834.6:c.9417G=	ENSP00000400883.3:p.Met3139=
NM_001144769.2:c.9951G=	NP_001138241.1:p.Met3317=
NM_001144770.1:c.9537G=	NP_001138242.1:p.Met3179=
NM_015548.4:c.8439G=	NP_056363.2:p.Met2813=
NM_183380.3:c.9417G=	NP_899236.1:p.Met3139=
XM_005249310.2:c.16308G=	XP_005249367.1:p.Met5436=
XM_005249315.2:c.16209G=	XP_005249372.1:p.Met5403=
XM_005249316.1:c.16023G=	XP_005249373.1:p.Met5341=
XM_005249318.1:c.15894G=	XP_005249375.1:p.Met5298=
XM_005249319.1:c.15795G=	XP_005249376.1:p.Met5265=
XM_005249320.3:c.15774G=	XP_005249377.1:p.Met5258=
XM_005249322.3:c.15753G=	XP_005249379.1:p.Met5251=
XM_005249323.2:c.15675G=	XP_005249380.1:p.Met5225=
XM_005249324.1:c.14697G=	XP_005249381.1:p.Met4899=
XM_011514824.1:c.16236G=	XP_011513126.1:p.Met5412=
XM_011514825.1:c.9978G=	XP_011513127.1:p.Met3326=
XM_011514826.1:c.15675G=	XP_011513128.1:p.Met5225=
XM_005249310.4:c.16308G=	XP_005249367.1:p.Met5436=
XM_005249315.3:c.16209G=	XP_005249372.1:p.Met5403=
XM_005249316.3:c.16023G=	XP_005249373.1:p.Met5341=
XM_005249318.2:c.15894G=	XP_005249375.1:p.Met5298=
XM_005249319.2:c.15795G=	XP_005249376.1:p.Met5265=
XM_005249320.4:c.15774G=	XP_005249377.1:p.Met5258=
XM_005249322.5:c.15753G=	XP_005249379.1:p.Met5251=
XM_005249323.4:c.15675G=	XP_005249380.1:p.Met5225=
XM_005249324.3:c.14697G=	XP_005249381.1:p.Met4899=
XM_011514824.2:c.16236G=	XP_011513126.1:p.Met5412=
XM_011514825.3:c.9978G=	XP_011513127.1:p.Met3326=
XM_011514826.3:c.15675G=	XP_011513128.1:p.Met5225=
XM_017011205.1:c.16335G=	XP_016866694.1:p.Met5445=
XM_017011206.1:c.16335G=	XP_016866695.1:p.Met5445=
XM_017011207.1:c.16272G=	XP_016866696.1:p.Met5424=
XM_017011208.1:c.16335G=	XP_016866697.1:p.Met5445=
XM_017011209.1:c.16335G=	XP_016866698.1:p.Met5445=
XM_017011210.1:c.16335G=	XP_016866699.1:p.Met5445=
XM_017011211.2:c.16335G=	XP_016866700.1:p.Met5445=
XM_017011212.1:c.16101G=	XP_016866701.1:p.Met5367=
XM_017011213.1:c.16335G=	XP_016866702.1:p.Met5445=
XM_017011214.2:c.16335G=	XP_016866703.1:p.Met5445=
XM_017011215.2:c.16335G=	XP_016866704.1:p.Met5445=
XM_017011216.2:c.16335G=	XP_016866705.1:p.Met5445=
XM_017011217.1:c.15711G=	XP_016866706.1:p.Met5237=
XM_017011218.1:c.10902G=	XP_016866707.1:p.Met3634=
XM_017011219.1:c.10077G=	XP_016866708.1:p.Met3359=
XM_017011220.1:c.9951G=	XP_016866709.1:p.Met3317=
XM_017011221.1:c.9843G=	XP_016866710.1:p.Met3281=
XM_017011222.2:c.9765G=	XP_016866711.1:p.Met3255=
XM_017011223.1:c.10077G=	XP_016866712.1:p.Met3359=
XM_017011224.2:c.9417G=	XP_016866713.1:p.Met3139=
XM_024446530.1:c.15654G=	XP_024302298.1:p.Met5218=
NM_001144769.5:c.9951G=	NP_001138241.1:p.Met3317=
NM_001144770.2:c.9537G=	NP_001138242.1:p.Met3179=
NM_001374722.1:c.16308G=	NP_001361651.1:p.Met5436=
NM_001374729.1:c.15675G=	NP_001361658.1:p.Met5225=
NM_001374730.1:c.9417G=	NP_001361659.1:p.Met3139=
NM_001374734.1:c.16335G=	NP_001361663.1:p.Met5445=
NM_001374736.1:c.16308G= MANE Select	NP_001361665.1:p.Met5436=
NM_015548.5:c.8439G=	NP_056363.2:p.Met2813=
NM_183380.4:c.9417G=	NP_899236.1:p.Met3139=
NM_001386100.1:c.9417G=	NP_001373029.1:p.Met3139=