Canonical Allele Identifier: CA381702585

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146883A>G (hg19) ; chr11:g.71435837A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435837A>G , CM000673.2:g.71435837A>G	GRCh38
NC_000011.9:g.71146883A>G , CM000673.1:g.71146883A>G	GRCh37
NC_000011.8:g.70824531A>G	NCBI36
NG_012655.2:g.17595T>C , LRG_340:g.17595T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.966T>C	ENSP00000435707.3:p.Gly322=
ENST00000526780.6:c.966T>C	ENSP00000435668.2:p.Gly322=
ENST00000527316.6:c.792T>C	ENSP00000435047.2:p.Gly264=
ENST00000682708.1:c.1017T>C	ENSP00000506866.1:p.Gly339=
ENST00000683287.1:c.1002T>C	ENSP00000507607.1:p.Gly334=
ENST00000683714.1:c.974T>C	ENSP00000508207.1:p.Val325Ala
ENST00000684396.1:n.1006T>C
ENST00000685320.1:c.381T>C	ENSP00000509319.1:p.Gly127=
ENST00000690257.1:c.870T>C	ENSP00000510750.1:p.Gly290=
ENST00000355527.8:c.966T>C MANE Select	ENSP00000347717.4:p.Gly322=
ENST00000355527.7:c.966T>C	ENSP00000347717.3:p.Gly322=
ENST00000407721.6:c.966T>C	ENSP00000384739.2:p.Gly322=
ENST00000525137.1:c.467T>C	ENSP00000435956.1:p.Val156Ala
ENST00000533800.5:c.216T>C	ENSP00000435011.1:p.Gly72=
ENST00000534795.5:c.319+1975T>C
NM_001163817.1:c.966T>C	NP_001157289.1:p.Gly322=
NM_001360.2:c.966T>C , LRG_340t1:c.966T>C	NP_001351.2:p.Gly322=
XM_011544777.1:c.1100T>C	XP_011543079.1:p.Val367Ala
XM_011544777.2:c.1100T>C	XP_011543079.1:p.Val367Ala
NM_001163817.2:c.966T>C	NP_001157289.1:p.Gly322=
NM_001360.3:c.966T>C MANE Select	NP_001351.2:p.Gly322=