Canonical Allele Identifier: CA381702353

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146818C>A (hg19) ; chr11:g.71435772C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435772C>A , CM000673.2:g.71435772C>A	GRCh38
NC_000011.9:g.71146818C>A , CM000673.1:g.71146818C>A	GRCh37
NC_000011.8:g.70824466C>A	NCBI36
NG_012655.2:g.17660G>T , LRG_340:g.17660G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1031G>T	ENSP00000435707.3:p.Gly344Val
ENST00000526780.6:c.1031G>T	ENSP00000435668.2:p.Gly344Val
ENST00000527316.6:c.857G>T	ENSP00000435047.2:p.Gly286Val
ENST00000682708.1:c.1082G>T	ENSP00000506866.1:p.Gly361Val
ENST00000683287.1:c.1067G>T	ENSP00000507607.1:p.Gly356Val
ENST00000683714.1:c.1039G>T	ENSP00000508207.1:p.Ala347Ser
ENST00000684396.1:n.1071G>T
ENST00000685320.1:c.446G>T	ENSP00000509319.1:p.Gly149Val
ENST00000690257.1:c.935G>T	ENSP00000510750.1:p.Gly312Val
ENST00000355527.8:c.1031G>T MANE Select	ENSP00000347717.4:p.Gly344Val
ENST00000355527.7:c.1031G>T	ENSP00000347717.3:p.Gly344Val
ENST00000407721.6:c.1031G>T	ENSP00000384739.2:p.Gly344Val
ENST00000525137.1:c.532G>T	ENSP00000435956.1:p.Ala178Ser
ENST00000533800.5:c.281G>T	ENSP00000435011.1:p.Gly94Val
ENST00000534795.5:c.319+2040G>T
NM_001163817.1:c.1031G>T	NP_001157289.1:p.Gly344Val
NM_001360.2:c.1031G>T , LRG_340t1:c.1031G>T	NP_001351.2:p.Gly344Val
XM_011544777.1:c.1165G>T	XP_011543079.1:p.Ala389Ser
XM_011544777.2:c.1165G>T	XP_011543079.1:p.Ala389Ser
NM_001163817.2:c.1031G>T	NP_001157289.1:p.Gly344Val
NM_001360.3:c.1031G>T MANE Select	NP_001351.2:p.Gly344Val