Canonical Allele Identifier: CA1981488026

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71437873T= , CM000673.2:g.71437873T=	GRCh38
NC_000011.9:g.71148919T= , CM000673.1:g.71148919T=	GRCh37
NC_000011.8:g.70826567T=	NCBI36
NG_012655.2:g.15559A= , LRG_340:g.15559A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.902A=	ENSP00000435707.3:p.His301=
ENST00000526780.6:c.902A=	ENSP00000435668.2:p.His301=
ENST00000527316.6:c.728A=	ENSP00000435047.2:p.His243=
ENST00000682708.1:c.953A=	ENSP00000506866.1:p.His318=
ENST00000682880.1:c.902A=	ENSP00000507520.1:p.His301=
ENST00000683287.1:c.938A=	ENSP00000507607.1:p.His313=
ENST00000683714.1:c.902A=	ENSP00000508207.1:p.His301=
ENST00000684396.1:n.942A=
ENST00000685320.1:c.317A=	ENSP00000509319.1:p.His106=
ENST00000690257.1:c.806A=	ENSP00000510750.1:p.His269=
ENST00000355527.8:c.902A= MANE Select	ENSP00000347717.4:p.His301=
ENST00000355527.7:c.902A=	ENSP00000347717.3:p.His301=
ENST00000407721.6:c.902A=	ENSP00000384739.2:p.His301=
ENST00000525137.1:c.269A=	ENSP00000435956.1:p.His90=
ENST00000533800.5:c.152A=	ENSP00000435011.1:p.His51=
ENST00000534795.5:c.258A=
NM_001163817.1:c.902A=	NP_001157289.1:p.His301=
NM_001360.2:c.902A= , LRG_340t1:c.902A=	NP_001351.2:p.His301=
XM_011544777.1:c.902A=	XP_011543079.1:p.His301=
XM_011544777.2:c.902A=	XP_011543079.1:p.His301=
NM_001163817.2:c.902A=	NP_001157289.1:p.His301=
NM_001360.3:c.902A= MANE Select	NP_001351.2:p.His301=