Canonical Allele Identifier: CA1981486878

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435547C= , CM000673.2:g.71435547C=	GRCh38
NC_000011.9:g.71146593C= , CM000673.1:g.71146593C=	GRCh37
NC_000011.8:g.70824241C=	NCBI36
NG_012655.2:g.17885G= , LRG_340:g.17885G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1256G=	ENSP00000435707.3:p.Cys419=
ENST00000526780.6:c.1256G=	ENSP00000435668.2:p.Cys419=
ENST00000527316.6:c.1082G=	ENSP00000435047.2:p.Cys361=
ENST00000682708.1:c.1307G=	ENSP00000506866.1:p.Cys436=
ENST00000683287.1:c.1292G=	ENSP00000507607.1:p.Cys431=
ENST00000683714.1:c.*19G=	ENSP00000508207.1:n.*19G=
ENST00000684396.1:n.1296G=
ENST00000685320.1:c.671G=	ENSP00000509319.1:p.Cys224=
ENST00000690257.1:c.1160G=	ENSP00000510750.1:p.Cys387=
ENST00000355527.8:c.1256G= MANE Select	ENSP00000347717.4:p.Cys419=
ENST00000355527.7:c.1256G=	ENSP00000347717.3:p.Cys419=
ENST00000407721.6:c.1256G=	ENSP00000384739.2:p.Cys419=
ENST00000525137.1:c.757G=	ENSP00000435956.1:n.757G=
ENST00000533800.5:c.506G=	ENSP00000435011.1:p.Cys169=
ENST00000534795.5:c.319+2265G=
NM_001163817.1:c.1256G=	NP_001157289.1:p.Cys419=
NM_001360.2:c.1256G= , LRG_340t1:c.1256G=	NP_001351.2:p.Cys419=
XM_011544777.1:c.*19G=	XP_011543079.1:n.*19G=
XM_011544777.2:c.*19G=	XP_011543079.1:n.*19G=
NM_001163817.2:c.1256G=	NP_001157289.1:p.Cys419=
NM_001360.3:c.1256G= MANE Select	NP_001351.2:p.Cys419=