Canonical Allele Identifier: CA475565658

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146454T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435408T>G , CM000673.2:g.71435408T>G	GRCh38
NC_000011.9:g.71146454T>G , CM000673.1:g.71146454T>G	GRCh37
NC_000011.8:g.70824102T>G	NCBI36
NG_012655.2:g.18024A>C , LRG_340:g.18024A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1395A>C	ENSP00000435707.3:p.Ala465=
ENST00000526780.6:c.1395A>C	ENSP00000435668.2:p.Ala465=
ENST00000527316.6:c.1221A>C	ENSP00000435047.2:p.Ala407=
ENST00000682708.1:c.1446A>C	ENSP00000506866.1:p.Ala482=
ENST00000683287.1:c.1431A>C	ENSP00000507607.1:p.Ala477=
ENST00000683714.1:c.*158A>C	ENSP00000508207.1:n.*158A>C
ENST00000684396.1:n.1435A>C
ENST00000685320.1:c.810A>C	ENSP00000509319.1:p.Ala270=
ENST00000690257.1:c.1299A>C	ENSP00000510750.1:p.Ala433=
ENST00000355527.8:c.1395A>C MANE Select	ENSP00000347717.4:p.Ala465=
ENST00000355527.7:c.1395A>C	ENSP00000347717.3:p.Ala465=
ENST00000407721.6:c.1395A>C	ENSP00000384739.2:p.Ala465=
ENST00000525137.1:c.896A>C	ENSP00000435956.1:n.896A>C
ENST00000533800.5:c.611+34A>C	ENSP00000435011.1:n.611+34A>C
ENST00000534795.5:c.319+2404A>C
NM_001163817.1:c.1395A>C	NP_001157289.1:p.Ala465=
NM_001360.2:c.1395A>C , LRG_340t1:c.1395A>C	NP_001351.2:p.Ala465=
XM_011544777.1:c.*158A>C	XP_011543079.1:n.*158A>C
XM_011544777.2:c.*158A>C	XP_011543079.1:n.*158A>C
NM_001163817.2:c.1395A>C	NP_001157289.1:p.Ala465=
NM_001360.3:c.1395A>C MANE Select	NP_001351.2:p.Ala465=