Canonical Allele Identifier: CA1981487549

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71436881G= , CM000673.2:g.71436881G=	GRCh38
NC_000011.9:g.71147927G= , CM000673.1:g.71147927G=	GRCh37
NC_000011.8:g.70825575G=	NCBI36
NG_012655.2:g.16551C= , LRG_340:g.16551C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000525346.6:c.963+931C=	ENSP00000435707.3:n.963+931C=
ENST00000526780.6:c.963+931C=	ENSP00000435668.2:n.963+931C=
ENST00000527316.6:c.789+931C=	ENSP00000435047.2:n.789+931C=
ENST00000682708.1:c.1014+931C=	ENSP00000506866.1:n.1014+931C=
ENST00000682880.1:c.*793C=	ENSP00000507520.1:n.*793C=
ENST00000683287.1:c.999+931C=	ENSP00000507607.1:n.999+931C=
ENST00000683714.1:c.971+923C=	ENSP00000508207.1:n.971+923C=
ENST00000684396.1:n.1003+931C=
ENST00000685320.1:c.378+931C=	ENSP00000509319.1:n.378+931C=
ENST00000690257.1:c.867+931C=	ENSP00000510750.1:n.867+931C=
ENST00000355527.8:c.963+931C= MANE Select	ENSP00000347717.4:n.963+931C=
ENST00000355527.7:c.963+931C=	ENSP00000347717.3:n.963+931C=
ENST00000407721.6:c.963+931C=	ENSP00000384739.2:n.963+931C=
ENST00000525137.1:c.331-908C=	ENSP00000435956.1:n.331-908C=
ENST00000533800.5:c.213+931C=	ENSP00000435011.1:n.213+931C=
ENST00000534795.5:c.319+931C=
NM_001163817.1:c.963+931C=	NP_001157289.1:n.963+931C=
NM_001360.2:c.963+931C= , LRG_340t1:c.963+931C=	NP_001351.2:n.963+931C=
XM_011544777.1:c.964-908C=	XP_011543079.1:n.964-908C=
XM_011544777.2:c.964-908C=	XP_011543079.1:n.964-908C=
NM_001163817.2:c.963+931C=	NP_001157289.1:n.963+931C=
NM_001360.3:c.963+931C= MANE Select	NP_001351.2:n.963+931C=