Canonical Allele Identifier: CA1981487002

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435747C= , CM000673.2:g.71435747C=	GRCh38
NC_000011.9:g.71146793C= , CM000673.1:g.71146793C=	GRCh37
NC_000011.8:g.70824441C=	NCBI36
NG_012655.2:g.17685G= , LRG_340:g.17685G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1056G=	ENSP00000435707.3:p.Arg352=
ENST00000526780.6:c.1056G=	ENSP00000435668.2:p.Arg352=
ENST00000527316.6:c.882G=	ENSP00000435047.2:p.Arg294=
ENST00000682708.1:c.1107G=	ENSP00000506866.1:p.Arg369=
ENST00000683287.1:c.1092G=	ENSP00000507607.1:p.Arg364=
ENST00000683714.1:c.1064G=	ENSP00000508207.1:p.Gly355=
ENST00000684396.1:n.1096G=
ENST00000685320.1:c.471G=	ENSP00000509319.1:p.Arg157=
ENST00000690257.1:c.960G=	ENSP00000510750.1:p.Arg320=
ENST00000355527.8:c.1056G= MANE Select	ENSP00000347717.4:p.Arg352=
ENST00000355527.7:c.1056G=	ENSP00000347717.3:p.Arg352=
ENST00000407721.6:c.1056G=	ENSP00000384739.2:p.Arg352=
ENST00000525137.1:c.557G=	ENSP00000435956.1:p.Gly186=
ENST00000533800.5:c.306G=	ENSP00000435011.1:p.Arg102=
ENST00000534795.5:c.319+2065G=
NM_001163817.1:c.1056G=	NP_001157289.1:p.Arg352=
NM_001360.2:c.1056G= , LRG_340t1:c.1056G=	NP_001351.2:p.Arg352=
XM_011544777.1:c.1190G=	XP_011543079.1:p.Gly397=
XM_011544777.2:c.1190G=	XP_011543079.1:p.Gly397=
NM_001163817.2:c.1056G=	NP_001157289.1:p.Arg352=
NM_001360.3:c.1056G= MANE Select	NP_001351.2:p.Arg352=