Canonical Allele Identifier: CA1981486984

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435725G= , CM000673.2:g.71435725G=	GRCh38
NC_000011.9:g.71146771G= , CM000673.1:g.71146771G=	GRCh37
NC_000011.8:g.70824419G=	NCBI36
NG_012655.2:g.17707C= , LRG_340:g.17707C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1078C=	ENSP00000435707.3:p.Leu360=
ENST00000526780.6:c.1078C=	ENSP00000435668.2:p.Leu360=
ENST00000527316.6:c.904C=	ENSP00000435047.2:p.Leu302=
ENST00000682708.1:c.1129C=	ENSP00000506866.1:p.Leu377=
ENST00000683287.1:c.1114C=	ENSP00000507607.1:p.Leu372=
ENST00000683714.1:c.1086C=	ENSP00000508207.1:p.Thr362=
ENST00000684396.1:n.1118C=
ENST00000685320.1:c.493C=	ENSP00000509319.1:p.Leu165=
ENST00000690257.1:c.982C=	ENSP00000510750.1:p.Leu328=
ENST00000355527.8:c.1078C= MANE Select	ENSP00000347717.4:p.Leu360=
ENST00000355527.7:c.1078C=	ENSP00000347717.3:p.Leu360=
ENST00000407721.6:c.1078C=	ENSP00000384739.2:p.Leu360=
ENST00000525137.1:c.579C=	ENSP00000435956.1:p.Thr193=
ENST00000533800.5:c.328C=	ENSP00000435011.1:p.Leu110=
ENST00000534795.5:c.319+2087C=
NM_001163817.1:c.1078C=	NP_001157289.1:p.Leu360=
NM_001360.2:c.1078C= , LRG_340t1:c.1078C=	NP_001351.2:p.Leu360=
XM_011544777.1:c.1212C=	XP_011543079.1:p.Thr404=
XM_011544777.2:c.1212C=	XP_011543079.1:p.Thr404=
NM_001163817.2:c.1078C=	NP_001157289.1:p.Leu360=
NM_001360.3:c.1078C= MANE Select	NP_001351.2:p.Leu360=