Canonical Allele Identifier: CA224324413

Gene: DHCR7

Linked Data

• dbSNP Id: rs975439299
• MyVariant Identifiers: chr11:g.71146753C>T (hg19) ; chr11:g.71435707C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435707C>T , CM000673.2:g.71435707C>T	GRCh38
NC_000011.9:g.71146753C>T , CM000673.1:g.71146753C>T	GRCh37
NC_000011.8:g.70824401C>T	NCBI36
NG_012655.2:g.17725G>A , LRG_340:g.17725G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1096G>A	ENSP00000435707.3:p.Gly366Arg
ENST00000526780.6:c.1096G>A	ENSP00000435668.2:p.Gly366Arg
ENST00000527316.6:c.922G>A	ENSP00000435047.2:p.Gly308Arg
ENST00000682708.1:c.1147G>A	ENSP00000506866.1:p.Gly383Arg
ENST00000683287.1:c.1132G>A	ENSP00000507607.1:p.Gly378Arg
ENST00000683714.1:c.1104G>A	ENSP00000508207.1:p.Met368Ile
ENST00000684396.1:n.1136G>A
ENST00000685320.1:c.511G>A	ENSP00000509319.1:p.Gly171Arg
ENST00000690257.1:c.1000G>A	ENSP00000510750.1:p.Gly334Arg
ENST00000355527.8:c.1096G>A MANE Select	ENSP00000347717.4:p.Gly366Arg
ENST00000355527.7:c.1096G>A	ENSP00000347717.3:p.Gly366Arg
ENST00000407721.6:c.1096G>A	ENSP00000384739.2:p.Gly366Arg
ENST00000525137.1:c.597G>A	ENSP00000435956.1:p.Met199Ile
ENST00000533800.5:c.346G>A	ENSP00000435011.1:p.Gly116Arg
ENST00000534795.5:c.319+2105G>A
NM_001163817.1:c.1096G>A	NP_001157289.1:p.Gly366Arg
NM_001360.2:c.1096G>A , LRG_340t1:c.1096G>A	NP_001351.2:p.Gly366Arg
XM_011544777.1:c.1230G>A	XP_011543079.1:p.Met410Ile
XM_011544777.2:c.1230G>A	XP_011543079.1:p.Met410Ile
NM_001163817.2:c.1096G>A	NP_001157289.1:p.Gly366Arg
NM_001360.3:c.1096G>A MANE Select	NP_001351.2:p.Gly366Arg