Canonical Allele Identifier: CA381701456

Gene: DHCR7

Linked Data

• ClinVar Variation Id: 2055638
• ClinVar RCV Id: RCV002938140
• MyVariant Identifiers: chr11:g.71146637G>A (hg19) ; chr11:g.71435591G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435591G>A , CM000673.2:g.71435591G>A	GRCh38
NC_000011.9:g.71146637G>A , CM000673.1:g.71146637G>A	GRCh37
NC_000011.8:g.70824285G>A	NCBI36
NG_012655.2:g.17841C>T , LRG_340:g.17841C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1212C>T	ENSP00000435707.3:p.Arg404=
ENST00000526780.6:c.1212C>T	ENSP00000435668.2:p.Arg404=
ENST00000527316.6:c.1038C>T	ENSP00000435047.2:p.Arg346=
ENST00000682708.1:c.1263C>T	ENSP00000506866.1:p.Arg421=
ENST00000683287.1:c.1248C>T	ENSP00000507607.1:p.Arg416=
ENST00000683714.1:c.1220C>T	ENSP00000508207.1:p.Ala407Val
ENST00000684396.1:n.1252C>T
ENST00000685320.1:c.627C>T	ENSP00000509319.1:p.Arg209=
ENST00000690257.1:c.1116C>T	ENSP00000510750.1:p.Arg372=
ENST00000355527.8:c.1212C>T MANE Select	ENSP00000347717.4:p.Arg404=
ENST00000355527.7:c.1212C>T	ENSP00000347717.3:p.Arg404=
ENST00000407721.6:c.1212C>T	ENSP00000384739.2:p.Arg404=
ENST00000525137.1:c.713C>T	ENSP00000435956.1:p.Ala238Val
ENST00000533800.5:c.462C>T	ENSP00000435011.1:p.Arg154=
ENST00000534795.5:c.319+2221C>T
NM_001163817.1:c.1212C>T	NP_001157289.1:p.Arg404=
NM_001360.2:c.1212C>T , LRG_340t1:c.1212C>T	NP_001351.2:p.Arg404=
XM_011544777.1:c.1346C>T	XP_011543079.1:p.Ala449Val
XM_011544777.2:c.1346C>T	XP_011543079.1:p.Ala449Val
NM_001163817.2:c.1212C>T	NP_001157289.1:p.Arg404=
NM_001360.3:c.1212C>T MANE Select	NP_001351.2:p.Arg404=