Canonical Allele Identifier: CA1981487006

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435751A= , CM000673.2:g.71435751A=	GRCh38
NC_000011.9:g.71146797A= , CM000673.1:g.71146797A=	GRCh37
NC_000011.8:g.70824445A=	NCBI36
NG_012655.2:g.17681T= , LRG_340:g.17681T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1052T=	ENSP00000435707.3:p.Phe351=
ENST00000526780.6:c.1052T=	ENSP00000435668.2:p.Phe351=
ENST00000527316.6:c.878T=	ENSP00000435047.2:p.Phe293=
ENST00000682708.1:c.1103T=	ENSP00000506866.1:p.Phe368=
ENST00000683287.1:c.1088T=	ENSP00000507607.1:p.Phe363=
ENST00000683714.1:c.1060T=	ENSP00000508207.1:p.Ser354=
ENST00000684396.1:n.1092T=
ENST00000685320.1:c.467T=	ENSP00000509319.1:p.Phe156=
ENST00000690257.1:c.956T=	ENSP00000510750.1:p.Phe319=
ENST00000355527.8:c.1052T= MANE Select	ENSP00000347717.4:p.Phe351=
ENST00000355527.7:c.1052T=	ENSP00000347717.3:p.Phe351=
ENST00000407721.6:c.1052T=	ENSP00000384739.2:p.Phe351=
ENST00000525137.1:c.553T=	ENSP00000435956.1:p.Ser185=
ENST00000533800.5:c.302T=	ENSP00000435011.1:p.Phe101=
ENST00000534795.5:c.319+2061T=
NM_001163817.1:c.1052T=	NP_001157289.1:p.Phe351=
NM_001360.2:c.1052T= , LRG_340t1:c.1052T=	NP_001351.2:p.Phe351=
XM_011544777.1:c.1186T=	XP_011543079.1:p.Ser396=
XM_011544777.2:c.1186T=	XP_011543079.1:p.Ser396=
NM_001163817.2:c.1052T=	NP_001157289.1:p.Phe351=
NM_001360.3:c.1052T= MANE Select	NP_001351.2:p.Phe351=