Canonical Allele Identifier: CA381694407

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71441286A>T , CM000673.2:g.71441286A>T	GRCh38
NC_000011.9:g.71152332A>T , CM000673.1:g.71152332A>T	GRCh37
NC_000011.8:g.70829980A>T	NCBI36
NG_012655.2:g.12146T>A , LRG_340:g.12146T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001360.3:c.567T>A MANE Select	NP_001351.2:p.Tyr189Ter
ENST00000355527.8:c.567T>A MANE Select	ENSP00000347717.4:p.Tyr189Ter
NM_001163817.1:c.567T>A	NP_001157289.1:p.Tyr189Ter
NM_001163817.2:c.567T>A	NP_001157289.1:p.Tyr189Ter
NM_001360.2:c.567T>A , LRG_340t1:c.567T>A	NP_001351.2:p.Tyr189Ter
ENST00000355527.7:c.567T>A	ENSP00000347717.3:p.Tyr189Ter
ENST00000407721.6:c.567T>A	ENSP00000384739.2:p.Tyr189Ter
ENST00000525346.6:c.567T>A	ENSP00000435707.3:p.Tyr189Ter
ENST00000526780.6:c.567T>A	ENSP00000435668.2:p.Tyr189Ter
ENST00000527316.5:c.471T>A	ENSP00000435047.1:p.Tyr157Ter
ENST00000527316.6:c.393T>A	ENSP00000435047.2:p.Tyr131Ter
ENST00000534701.1:n.62T>A
ENST00000682708.1:c.567T>A	ENSP00000506866.1:p.Tyr189Ter
ENST00000682880.1:c.567T>A	ENSP00000507520.1:p.Tyr189Ter
ENST00000683287.1:c.603T>A	ENSP00000507607.1:p.Tyr201Ter
ENST00000683714.1:c.567T>A	ENSP00000508207.1:p.Tyr189Ter
ENST00000683874.1:n.844T>A
ENST00000685320.1:c.-19T>A	ENSP00000509319.1:n.-19T>A
ENST00000690257.1:c.471T>A	ENSP00000510750.1:p.Tyr157Ter
XM_011544777.1:c.567T>A	XP_011543079.1:p.Tyr189Ter
XM_011544777.2:c.567T>A	XP_011543079.1:p.Tyr189Ter