Canonical Allele Identifier: CA1981488637

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71439084C= , CM000673.2:g.71439084C=	GRCh38
NC_000011.9:g.71150130C= , CM000673.1:g.71150130C=	GRCh37
NC_000011.8:g.70827778C=	NCBI36
NG_012655.2:g.14348G= , LRG_340:g.14348G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001360.3:c.627-1G= MANE Select	NP_001351.2:n.627-1G=
ENST00000355527.8:c.627-1G= MANE Select	ENSP00000347717.4:n.627-1G=
NM_001163817.1:c.627-1G=	NP_001157289.1:n.627-1G=
NM_001163817.2:c.627-1G=	NP_001157289.1:n.627-1G=
NM_001360.2:c.627-1G= , LRG_340t1:c.627-1G=	NP_001351.2:n.627-1G=
ENST00000355527.7:c.627-1G=	ENSP00000347717.3:n.627-1G=
ENST00000407721.6:c.627-1G=	ENSP00000384739.2:n.627-1G=
ENST00000525346.6:c.627-1G=	ENSP00000435707.3:n.627-1G=
ENST00000526780.6:c.627-1G=	ENSP00000435668.2:n.627-1G=
ENST00000527316.5:c.531-1G=	ENSP00000435047.1:n.531-1G=
ENST00000527316.6:c.453-1G=	ENSP00000435047.2:n.453-1G=
ENST00000534701.1:n.122-1G=
ENST00000682708.1:c.678-1G=	ENSP00000506866.1:n.678-1G=
ENST00000682880.1:c.627-1G=	ENSP00000507520.1:n.627-1G=
ENST00000683287.1:c.663-1G=	ENSP00000507607.1:n.663-1G=
ENST00000683714.1:c.627-1G=	ENSP00000508207.1:n.627-1G=
ENST00000684396.1:n.666G=
ENST00000685320.1:c.42-1G=	ENSP00000509319.1:n.42-1G=
ENST00000690257.1:c.531-1G=	ENSP00000510750.1:n.531-1G=
XM_011544777.1:c.627-1G=	XP_011543079.1:n.627-1G=
XM_011544777.2:c.627-1G=	XP_011543079.1:n.627-1G=