Canonical Allele Identifier: CA1981486978

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435718C= , CM000673.2:g.71435718C=	GRCh38
NC_000011.9:g.71146764C= , CM000673.1:g.71146764C=	GRCh37
NC_000011.8:g.70824412C=	NCBI36
NG_012655.2:g.17714G= , LRG_340:g.17714G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1085G=	ENSP00000435707.3:p.Arg362=
ENST00000526780.6:c.1085G=	ENSP00000435668.2:p.Arg362=
ENST00000527316.6:c.911G=	ENSP00000435047.2:p.Arg304=
ENST00000682708.1:c.1136G=	ENSP00000506866.1:p.Arg379=
ENST00000683287.1:c.1121G=	ENSP00000507607.1:p.Arg374=
ENST00000683714.1:c.1093G=	ENSP00000508207.1:p.Ala365=
ENST00000684396.1:n.1125G=
ENST00000685320.1:c.500G=	ENSP00000509319.1:p.Arg167=
ENST00000690257.1:c.989G=	ENSP00000510750.1:p.Arg330=
ENST00000355527.8:c.1085G= MANE Select	ENSP00000347717.4:p.Arg362=
ENST00000355527.7:c.1085G=	ENSP00000347717.3:p.Arg362=
ENST00000407721.6:c.1085G=	ENSP00000384739.2:p.Arg362=
ENST00000525137.1:c.586G=	ENSP00000435956.1:p.Ala196=
ENST00000533800.5:c.335G=	ENSP00000435011.1:p.Arg112=
ENST00000534795.5:c.319+2094G=
NM_001163817.1:c.1085G=	NP_001157289.1:p.Arg362=
NM_001360.2:c.1085G= , LRG_340t1:c.1085G=	NP_001351.2:p.Arg362=
XM_011544777.1:c.1219G=	XP_011543079.1:p.Ala407=
XM_011544777.2:c.1219G=	XP_011543079.1:p.Ala407=
NM_001163817.2:c.1085G=	NP_001157289.1:p.Arg362=
NM_001360.3:c.1085G= MANE Select	NP_001351.2:p.Arg362=