Canonical Allele Identifier: CA1981486884

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435560T= , CM000673.2:g.71435560T=	GRCh38
NC_000011.9:g.71146606T= , CM000673.1:g.71146606T=	GRCh37
NC_000011.8:g.70824254T=	NCBI36
NG_012655.2:g.17872A= , LRG_340:g.17872A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1243A=	ENSP00000435707.3:p.Ser415=
ENST00000526780.6:c.1243A=	ENSP00000435668.2:p.Ser415=
ENST00000527316.6:c.1069A=	ENSP00000435047.2:p.Ser357=
ENST00000682708.1:c.1294A=	ENSP00000506866.1:p.Ser432=
ENST00000683287.1:c.1279A=	ENSP00000507607.1:p.Ser427=
ENST00000683714.1:c.*6A=	ENSP00000508207.1:n.*6A=
ENST00000684396.1:n.1283A=
ENST00000685320.1:c.658A=	ENSP00000509319.1:p.Ser220=
ENST00000690257.1:c.1147A=	ENSP00000510750.1:p.Ser383=
ENST00000355527.8:c.1243A= MANE Select	ENSP00000347717.4:p.Ser415=
ENST00000355527.7:c.1243A=	ENSP00000347717.3:p.Ser415=
ENST00000407721.6:c.1243A=	ENSP00000384739.2:p.Ser415=
ENST00000525137.1:c.744A=	ENSP00000435956.1:n.744A=
ENST00000533800.5:c.493A=	ENSP00000435011.1:p.Ser165=
ENST00000534795.5:c.319+2252A=
NM_001163817.1:c.1243A=	NP_001157289.1:p.Ser415=
NM_001360.2:c.1243A= , LRG_340t1:c.1243A=	NP_001351.2:p.Ser415=
XM_011544777.1:c.*6A=	XP_011543079.1:n.*6A=
XM_011544777.2:c.*6A=	XP_011543079.1:n.*6A=
NM_001163817.2:c.1243A=	NP_001157289.1:p.Ser415=
NM_001360.3:c.1243A= MANE Select	NP_001351.2:p.Ser415=