Canonical Allele Identifier: CA1981486770

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435371G= , CM000673.2:g.71435371G=	GRCh38
NC_000011.9:g.71146417G= , CM000673.1:g.71146417G=	GRCh37
NC_000011.8:g.70824065G=	NCBI36
NG_012655.2:g.18061C= , LRG_340:g.18061C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.*4C=	ENSP00000435707.3:n.*4C=
ENST00000526780.6:c.*4C=	ENSP00000435668.2:n.*4C=
ENST00000682708.1:c.*4C=	ENSP00000506866.1:n.*4C=
ENST00000683287.1:c.*4C=	ENSP00000507607.1:n.*4C=
ENST00000683714.1:c.*195C=	ENSP00000508207.1:n.*195C=
ENST00000684396.1:n.1472C=
ENST00000685320.1:c.*4C=	ENSP00000509319.1:n.*4C=
ENST00000690257.1:c.*4C=	ENSP00000510750.1:n.*4C=
ENST00000355527.8:c.*4C= MANE Select	ENSP00000347717.4:n.*4C=
ENST00000355527.7:c.*4C=	ENSP00000347717.3:n.*4C=
ENST00000407721.6:c.*4C=	ENSP00000384739.2:n.*4C=
ENST00000525137.1:c.933C=	ENSP00000435956.1:n.933C=
ENST00000533800.5:c.611+71C=	ENSP00000435011.1:n.611+71C=
ENST00000534795.5:c.319+2441C=
NM_001163817.1:c.*4C=	NP_001157289.1:n.*4C=
NM_001360.2:c.*4C= , LRG_340t1:c.*4C=	NP_001351.2:n.*4C=
XM_011544777.1:c.*195C=	XP_011543079.1:n.*195C=
XM_011544777.2:c.*195C=	XP_011543079.1:n.*195C=
NM_001163817.2:c.*4C=	NP_001157289.1:n.*4C=
NM_001360.3:c.*4C= MANE Select	NP_001351.2:n.*4C=