Canonical Allele Identifier: CA450620375

Gene: DST

Linked Data

• MyVariant Identifiers: chr6:g.56420438A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.56555640A>C , CM000668.2:g.56555640A>C	GRCh38
NC_000006.11:g.56420438A>C , CM000668.1:g.56420438A>C	GRCh37
NC_000006.10:g.56528397A>C	NCBI36
NG_029322.1:g.92257T>G
NG_029322.2:g.403989T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000421834.7:c.7950T>G	ENSP00000400883.3:p.Val2650=
ENST00000449297.7:c.8484T>G	ENSP00000393082.3:p.Val2828=
ENST00000520645.6:c.8070T>G	ENSP00000431030.2:p.Val2690=
ENST00000520144.2:n.812T>G
ENST00000680361.1:c.14841T>G MANE Select	ENSP00000505098.1:p.Val4947=
ENST00000244364.10:c.6972T>G	ENSP00000244364.6:p.Val2324=
ENST00000312431.10:c.8070T>G	ENSP00000307959.7:p.Val2690=
ENST00000361203.7:c.14208T>G	ENSP00000354508.3:p.Val4736=
ENST00000370754.9:c.8484T>G	ENSP00000359790.6:p.Val2828=
ENST00000370788.6:c.7950T>G	ENSP00000359824.2:p.Val2650=
ENST00000421834.6:c.7950T>G	ENSP00000400883.3:p.Val2650=
ENST00000520144.1:n.550T>G
NM_001144769.2:c.8484T>G	NP_001138241.1:p.Val2828=
NM_001144770.1:c.8070T>G	NP_001138242.1:p.Val2690=
NM_015548.4:c.6972T>G	NP_056363.2:p.Val2324=
NM_183380.3:c.7950T>G	NP_899236.1:p.Val2650=
XM_005249310.2:c.14841T>G	XP_005249367.1:p.Val4947=
XM_005249315.2:c.14742T>G	XP_005249372.1:p.Val4914=
XM_005249316.1:c.14556T>G	XP_005249373.1:p.Val4852=
XM_005249318.1:c.14427T>G	XP_005249375.1:p.Val4809=
XM_005249319.1:c.14328T>G	XP_005249376.1:p.Val4776=
XM_005249320.3:c.14307T>G	XP_005249377.1:p.Val4769=
XM_005249322.3:c.14286T>G	XP_005249379.1:p.Val4762=
XM_005249323.2:c.14208T>G	XP_005249380.1:p.Val4736=
XM_005249324.1:c.13230T>G	XP_005249381.1:p.Val4410=
XM_011514824.1:c.14769T>G	XP_011513126.1:p.Val4923=
XM_011514825.1:c.8511T>G	XP_011513127.1:p.Val2837=
XM_011514826.1:c.14208T>G	XP_011513128.1:p.Val4736=
XM_005249310.4:c.14841T>G	XP_005249367.1:p.Val4947=
XM_005249315.3:c.14742T>G	XP_005249372.1:p.Val4914=
XM_005249316.3:c.14556T>G	XP_005249373.1:p.Val4852=
XM_005249318.2:c.14427T>G	XP_005249375.1:p.Val4809=
XM_005249319.2:c.14328T>G	XP_005249376.1:p.Val4776=
XM_005249320.4:c.14307T>G	XP_005249377.1:p.Val4769=
XM_005249322.5:c.14286T>G	XP_005249379.1:p.Val4762=
XM_005249323.4:c.14208T>G	XP_005249380.1:p.Val4736=
XM_005249324.3:c.13230T>G	XP_005249381.1:p.Val4410=
XM_011514824.2:c.14769T>G	XP_011513126.1:p.Val4923=
XM_011514825.3:c.8511T>G	XP_011513127.1:p.Val2837=
XM_011514826.3:c.14208T>G	XP_011513128.1:p.Val4736=
XM_017011205.1:c.14868T>G	XP_016866694.1:p.Val4956=
XM_017011206.1:c.14868T>G	XP_016866695.1:p.Val4956=
XM_017011207.1:c.14805T>G	XP_016866696.1:p.Val4935=
XM_017011208.1:c.14868T>G	XP_016866697.1:p.Val4956=
XM_017011209.1:c.14868T>G	XP_016866698.1:p.Val4956=
XM_017011210.1:c.14868T>G	XP_016866699.1:p.Val4956=
XM_017011211.2:c.14868T>G	XP_016866700.1:p.Val4956=
XM_017011212.1:c.14634T>G	XP_016866701.1:p.Val4878=
XM_017011213.1:c.14868T>G	XP_016866702.1:p.Val4956=
XM_017011214.2:c.14868T>G	XP_016866703.1:p.Val4956=
XM_017011215.2:c.14868T>G	XP_016866704.1:p.Val4956=
XM_017011216.2:c.14868T>G	XP_016866705.1:p.Val4956=
XM_017011217.1:c.14244T>G	XP_016866706.1:p.Val4748=
XM_017011218.1:c.9435T>G	XP_016866707.1:p.Val3145=
XM_017011219.1:c.8610T>G	XP_016866708.1:p.Val2870=
XM_017011220.1:c.8484T>G	XP_016866709.1:p.Val2828=
XM_017011221.1:c.8376T>G	XP_016866710.1:p.Val2792=
XM_017011222.2:c.8298T>G	XP_016866711.1:p.Val2766=
XM_017011223.1:c.8610T>G	XP_016866712.1:p.Val2870=
XM_017011224.2:c.7950T>G	XP_016866713.1:p.Val2650=
XM_024446530.1:c.14187T>G	XP_024302298.1:p.Val4729=
NM_001144769.5:c.8484T>G	NP_001138241.1:p.Val2828=
NM_001144770.2:c.8070T>G	NP_001138242.1:p.Val2690=
NM_001374722.1:c.14841T>G	NP_001361651.1:p.Val4947=
NM_001374729.1:c.14208T>G	NP_001361658.1:p.Val4736=
NM_001374730.1:c.7950T>G	NP_001361659.1:p.Val2650=
NM_001374734.1:c.14868T>G	NP_001361663.1:p.Val4956=
NM_001374736.1:c.14841T>G MANE Select	NP_001361665.1:p.Val4947=
NM_015548.5:c.6972T>G	NP_056363.2:p.Val2324=
NM_183380.4:c.7950T>G	NP_899236.1:p.Val2650=
NM_001386100.1:c.7950T>G	NP_001373029.1:p.Val2650=