Canonical Allele Identifier: CA381703018

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71148922T>A (hg19) ; chr11:g.71437876T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71437876T>A , CM000673.2:g.71437876T>A	GRCh38
NC_000011.9:g.71148922T>A , CM000673.1:g.71148922T>A	GRCh37
NC_000011.8:g.70826570T>A	NCBI36
NG_012655.2:g.15556A>T , LRG_340:g.15556A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.899A>T	ENSP00000435707.3:p.Asp300Val
ENST00000526780.6:c.899A>T	ENSP00000435668.2:p.Asp300Val
ENST00000527316.6:c.725A>T	ENSP00000435047.2:p.Asp242Val
ENST00000682708.1:c.950A>T	ENSP00000506866.1:p.Asp317Val
ENST00000682880.1:c.899A>T	ENSP00000507520.1:p.Asp300Val
ENST00000683287.1:c.935A>T	ENSP00000507607.1:p.Asp312Val
ENST00000683714.1:c.899A>T	ENSP00000508207.1:p.Asp300Val
ENST00000684396.1:n.939A>T
ENST00000685320.1:c.314A>T	ENSP00000509319.1:p.Asp105Val
ENST00000690257.1:c.803A>T	ENSP00000510750.1:p.Asp268Val
ENST00000355527.8:c.899A>T MANE Select	ENSP00000347717.4:p.Asp300Val
ENST00000355527.7:c.899A>T	ENSP00000347717.3:p.Asp300Val
ENST00000407721.6:c.899A>T	ENSP00000384739.2:p.Asp300Val
ENST00000525137.1:c.266A>T	ENSP00000435956.1:p.Asp89Val
ENST00000533800.5:c.149A>T	ENSP00000435011.1:p.Asp50Val
ENST00000534795.5:c.255A>T
NM_001163817.1:c.899A>T	NP_001157289.1:p.Asp300Val
NM_001360.2:c.899A>T , LRG_340t1:c.899A>T	NP_001351.2:p.Asp300Val
XM_011544777.1:c.899A>T	XP_011543079.1:p.Asp300Val
XM_011544777.2:c.899A>T	XP_011543079.1:p.Asp300Val
NM_001163817.2:c.899A>T	NP_001157289.1:p.Asp300Val
NM_001360.3:c.899A>T MANE Select	NP_001351.2:p.Asp300Val