Canonical Allele Identifier: CA1981488022

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71437861T= , CM000673.2:g.71437861T=	GRCh38
NC_000011.9:g.71148907T= , CM000673.1:g.71148907T=	GRCh37
NC_000011.8:g.70826555T=	NCBI36
NG_012655.2:g.15571A= , LRG_340:g.15571A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.914A=	ENSP00000435707.3:p.Tyr305=
ENST00000526780.6:c.914A=	ENSP00000435668.2:p.Tyr305=
ENST00000527316.6:c.740A=	ENSP00000435047.2:p.Tyr247=
ENST00000682708.1:c.965A=	ENSP00000506866.1:p.Tyr322=
ENST00000682880.1:c.914A=	ENSP00000507520.1:p.Tyr305=
ENST00000683287.1:c.950A=	ENSP00000507607.1:p.Tyr317=
ENST00000683714.1:c.914A=	ENSP00000508207.1:p.Tyr305=
ENST00000684396.1:n.954A=
ENST00000685320.1:c.329A=	ENSP00000509319.1:p.Tyr110=
ENST00000690257.1:c.818A=	ENSP00000510750.1:p.Tyr273=
ENST00000355527.8:c.914A= MANE Select	ENSP00000347717.4:p.Tyr305=
ENST00000355527.7:c.914A=	ENSP00000347717.3:p.Tyr305=
ENST00000407721.6:c.914A=	ENSP00000384739.2:p.Tyr305=
ENST00000525137.1:c.281A=	ENSP00000435956.1:p.Tyr94=
ENST00000533800.5:c.164A=	ENSP00000435011.1:p.Tyr55=
ENST00000534795.5:c.270A=
NM_001163817.1:c.914A=	NP_001157289.1:p.Tyr305=
NM_001360.2:c.914A= , LRG_340t1:c.914A=	NP_001351.2:p.Tyr305=
XM_011544777.1:c.914A=	XP_011543079.1:p.Tyr305=
XM_011544777.2:c.914A=	XP_011543079.1:p.Tyr305=
NM_001163817.2:c.914A=	NP_001157289.1:p.Tyr305=
NM_001360.3:c.914A= MANE Select	NP_001351.2:p.Tyr305=