Canonical Allele Identifier: CA2739373812
Gene: DHCR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.71443985C>T , CM000673.2:g.71443985C>T GRCh38
NC_000011.9:g.71155031C>T , CM000673.1:g.71155031C>T GRCh37
NC_000011.8:g.70832679C>T NCBI36
NG_012655.2:g.9447G>A , LRG_340:g.9447G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000525346.6:c.321+8G>A ENSP00000435707.3:n.321+8G>A
ENST00000526780.6:c.321+8G>A ENSP00000435668.2:n.321+8G>A
ENST00000527316.6:c.147+8G>A ENSP00000435047.2:n.147+8G>A
ENST00000682708.1:c.321+8G>A ENSP00000506866.1:n.321+8G>A
ENST00000682880.1:c.321+8G>A ENSP00000507520.1:n.321+8G>A
ENST00000683287.1:c.329G>A ENSP00000507607.1:p.Ser110Asn
ENST00000683714.1:c.321+8G>A ENSP00000508207.1:n.321+8G>A
ENST00000683874.1:n.598+8G>A
ENST00000685320.1:c.-265+8G>A ENSP00000509319.1:n.-265+8G>A
ENST00000690257.1:c.225+8G>A ENSP00000510750.1:n.225+8G>A
ENST00000355527.8:c.321+8G>A MANE Select ENSP00000347717.4:n.321+8G>A
ENST00000355527.7:c.321+8G>A ENSP00000347717.3:n.321+8G>A
ENST00000407721.6:c.321+8G>A ENSP00000384739.2:n.321+8G>A
ENST00000526780.5:c.321+8G>A ENSP00000435668.1:n.321+8G>A
ENST00000527316.5:c.225+8G>A ENSP00000435047.1:n.225+8G>A
NM_001163817.1:c.321+8G>A NP_001157289.1:n.321+8G>A
NM_001360.2:c.321+8G>A , LRG_340t1:c.321+8G>A NP_001351.2:n.321+8G>A
XM_011544777.1:c.321+8G>A XP_011543079.1:n.321+8G>A
XM_011544777.2:c.321+8G>A XP_011543079.1:n.321+8G>A
NM_001163817.2:c.321+8G>A NP_001157289.1:n.321+8G>A
NM_001360.3:c.321+8G>A MANE Select NP_001351.2:n.321+8G>A