Canonical Allele Identifier: CA2739373809

Gene: DHCR7

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71443983G>T , CM000673.2:g.71443983G>T	GRCh38
NC_000011.9:g.71155029G>T , CM000673.1:g.71155029G>T	GRCh37
NC_000011.8:g.70832677G>T	NCBI36
NG_012655.2:g.9449C>A , LRG_340:g.9449C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.321+10C>A	ENSP00000435707.3:n.321+10C>A
ENST00000526780.6:c.321+10C>A	ENSP00000435668.2:n.321+10C>A
ENST00000527316.6:c.147+10C>A	ENSP00000435047.2:n.147+10C>A
ENST00000682708.1:c.321+10C>A	ENSP00000506866.1:n.321+10C>A
ENST00000682880.1:c.321+10C>A	ENSP00000507520.1:n.321+10C>A
ENST00000683287.1:c.331C>A	ENSP00000507607.1:p.Pro111Thr
ENST00000683714.1:c.321+10C>A	ENSP00000508207.1:n.321+10C>A
ENST00000683874.1:n.598+10C>A
ENST00000685320.1:c.-265+10C>A	ENSP00000509319.1:n.-265+10C>A
ENST00000690257.1:c.225+10C>A	ENSP00000510750.1:n.225+10C>A
ENST00000355527.8:c.321+10C>A MANE Select	ENSP00000347717.4:n.321+10C>A
ENST00000355527.7:c.321+10C>A	ENSP00000347717.3:n.321+10C>A
ENST00000407721.6:c.321+10C>A	ENSP00000384739.2:n.321+10C>A
ENST00000526780.5:c.321+10C>A	ENSP00000435668.1:n.321+10C>A
ENST00000527316.5:c.225+10C>A	ENSP00000435047.1:n.225+10C>A
NM_001163817.1:c.321+10C>A	NP_001157289.1:n.321+10C>A
NM_001360.2:c.321+10C>A , LRG_340t1:c.321+10C>A	NP_001351.2:n.321+10C>A
XM_011544777.1:c.321+10C>A	XP_011543079.1:n.321+10C>A
XM_011544777.2:c.321+10C>A	XP_011543079.1:n.321+10C>A
NM_001163817.2:c.321+10C>A	NP_001157289.1:n.321+10C>A
NM_001360.3:c.321+10C>A MANE Select	NP_001351.2:n.321+10C>A