Canonical Allele Identifier: CA364519794

Gene: DST

Linked Data

• MyVariant Identifiers: chr6:g.56420547G>T (hg19) ; chr6:g.56555749G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.56555749G>T , CM000668.2:g.56555749G>T	GRCh38
NC_000006.11:g.56420547G>T , CM000668.1:g.56420547G>T	GRCh37
NC_000006.10:g.56528506G>T	NCBI36
NG_029322.1:g.92148C>A
NG_029322.2:g.403880C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000421834.7:c.7841C>A	ENSP00000400883.3:p.Pro2614His
ENST00000449297.7:c.8375C>A	ENSP00000393082.3:p.Pro2792His
ENST00000520645.6:c.7961C>A	ENSP00000431030.2:p.Pro2654His
ENST00000520144.2:n.703C>A
ENST00000680361.1:c.14732C>A MANE Select	ENSP00000505098.1:p.Pro4911His
ENST00000244364.10:c.6863C>A	ENSP00000244364.6:p.Pro2288His
ENST00000312431.10:c.7961C>A	ENSP00000307959.7:p.Pro2654His
ENST00000361203.7:c.14099C>A	ENSP00000354508.3:p.Pro4700His
ENST00000370754.9:c.8375C>A	ENSP00000359790.6:p.Pro2792His
ENST00000370788.6:c.7841C>A	ENSP00000359824.2:p.Pro2614His
ENST00000421834.6:c.7841C>A	ENSP00000400883.3:p.Pro2614His
ENST00000520144.1:n.441C>A
NM_001144769.2:c.8375C>A	NP_001138241.1:p.Pro2792His
NM_001144770.1:c.7961C>A	NP_001138242.1:p.Pro2654His
NM_015548.4:c.6863C>A	NP_056363.2:p.Pro2288His
NM_183380.3:c.7841C>A	NP_899236.1:p.Pro2614His
XM_005249310.2:c.14732C>A	XP_005249367.1:p.Pro4911His
XM_005249315.2:c.14633C>A	XP_005249372.1:p.Pro4878His
XM_005249316.1:c.14447C>A	XP_005249373.1:p.Pro4816His
XM_005249318.1:c.14318C>A	XP_005249375.1:p.Pro4773His
XM_005249319.1:c.14219C>A	XP_005249376.1:p.Pro4740His
XM_005249320.3:c.14198C>A	XP_005249377.1:p.Pro4733His
XM_005249322.3:c.14177C>A	XP_005249379.1:p.Pro4726His
XM_005249323.2:c.14099C>A	XP_005249380.1:p.Pro4700His
XM_005249324.1:c.13121C>A	XP_005249381.1:p.Pro4374His
XM_011514824.1:c.14660C>A	XP_011513126.1:p.Pro4887His
XM_011514825.1:c.8402C>A	XP_011513127.1:p.Pro2801His
XM_011514826.1:c.14099C>A	XP_011513128.1:p.Pro4700His
XM_005249310.4:c.14732C>A	XP_005249367.1:p.Pro4911His
XM_005249315.3:c.14633C>A	XP_005249372.1:p.Pro4878His
XM_005249316.3:c.14447C>A	XP_005249373.1:p.Pro4816His
XM_005249318.2:c.14318C>A	XP_005249375.1:p.Pro4773His
XM_005249319.2:c.14219C>A	XP_005249376.1:p.Pro4740His
XM_005249320.4:c.14198C>A	XP_005249377.1:p.Pro4733His
XM_005249322.5:c.14177C>A	XP_005249379.1:p.Pro4726His
XM_005249323.4:c.14099C>A	XP_005249380.1:p.Pro4700His
XM_005249324.3:c.13121C>A	XP_005249381.1:p.Pro4374His
XM_011514824.2:c.14660C>A	XP_011513126.1:p.Pro4887His
XM_011514825.3:c.8402C>A	XP_011513127.1:p.Pro2801His
XM_011514826.3:c.14099C>A	XP_011513128.1:p.Pro4700His
XM_017011205.1:c.14759C>A	XP_016866694.1:p.Pro4920His
XM_017011206.1:c.14759C>A	XP_016866695.1:p.Pro4920His
XM_017011207.1:c.14696C>A	XP_016866696.1:p.Pro4899His
XM_017011208.1:c.14759C>A	XP_016866697.1:p.Pro4920His
XM_017011209.1:c.14759C>A	XP_016866698.1:p.Pro4920His
XM_017011210.1:c.14759C>A	XP_016866699.1:p.Pro4920His
XM_017011211.2:c.14759C>A	XP_016866700.1:p.Pro4920His
XM_017011212.1:c.14525C>A	XP_016866701.1:p.Pro4842His
XM_017011213.1:c.14759C>A	XP_016866702.1:p.Pro4920His
XM_017011214.2:c.14759C>A	XP_016866703.1:p.Pro4920His
XM_017011215.2:c.14759C>A	XP_016866704.1:p.Pro4920His
XM_017011216.2:c.14759C>A	XP_016866705.1:p.Pro4920His
XM_017011217.1:c.14135C>A	XP_016866706.1:p.Pro4712His
XM_017011218.1:c.9326C>A	XP_016866707.1:p.Pro3109His
XM_017011219.1:c.8501C>A	XP_016866708.1:p.Pro2834His
XM_017011220.1:c.8375C>A	XP_016866709.1:p.Pro2792His
XM_017011221.1:c.8267C>A	XP_016866710.1:p.Pro2756His
XM_017011222.2:c.8189C>A	XP_016866711.1:p.Pro2730His
XM_017011223.1:c.8501C>A	XP_016866712.1:p.Pro2834His
XM_017011224.2:c.7841C>A	XP_016866713.1:p.Pro2614His
XM_024446530.1:c.14078C>A	XP_024302298.1:p.Pro4693His
NM_001144769.5:c.8375C>A	NP_001138241.1:p.Pro2792His
NM_001144770.2:c.7961C>A	NP_001138242.1:p.Pro2654His
NM_001374722.1:c.14732C>A	NP_001361651.1:p.Pro4911His
NM_001374729.1:c.14099C>A	NP_001361658.1:p.Pro4700His
NM_001374730.1:c.7841C>A	NP_001361659.1:p.Pro2614His
NM_001374734.1:c.14759C>A	NP_001361663.1:p.Pro4920His
NM_001374736.1:c.14732C>A MANE Select	NP_001361665.1:p.Pro4911His
NM_015548.5:c.6863C>A	NP_056363.2:p.Pro2288His
NM_183380.4:c.7841C>A	NP_899236.1:p.Pro2614His
NM_001386100.1:c.7841C>A	NP_001373029.1:p.Pro2614His