Canonical Allele Identifier: CA381700602

Gene: DHCR7

Linked Data

• gnomAD v4: 11-71435431-C-T
• MyVariant Identifiers: chr11:g.71146477C>T (hg19) ; chr11:g.71435431C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435431C>T , CM000673.2:g.71435431C>T	GRCh38
NC_000011.9:g.71146477C>T , CM000673.1:g.71146477C>T	GRCh37
NC_000011.8:g.70824125C>T	NCBI36
NG_012655.2:g.18001G>A , LRG_340:g.18001G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1372G>A	ENSP00000435707.3:p.Asp458Asn
ENST00000526780.6:c.1372G>A	ENSP00000435668.2:p.Asp458Asn
ENST00000527316.6:c.1198G>A	ENSP00000435047.2:p.Asp400Asn
ENST00000682708.1:c.1423G>A	ENSP00000506866.1:p.Asp475Asn
ENST00000683287.1:c.1408G>A	ENSP00000507607.1:p.Asp470Asn
ENST00000683714.1:c.*135G>A	ENSP00000508207.1:n.*135G>A
ENST00000684396.1:n.1412G>A
ENST00000685320.1:c.787G>A	ENSP00000509319.1:p.Asp263Asn
ENST00000690257.1:c.1276G>A	ENSP00000510750.1:p.Asp426Asn
ENST00000355527.8:c.1372G>A MANE Select	ENSP00000347717.4:p.Asp458Asn
ENST00000355527.7:c.1372G>A	ENSP00000347717.3:p.Asp458Asn
ENST00000407721.6:c.1372G>A	ENSP00000384739.2:p.Asp458Asn
ENST00000525137.1:c.873G>A	ENSP00000435956.1:n.873G>A
ENST00000533800.5:c.611+11G>A	ENSP00000435011.1:n.611+11G>A
ENST00000534795.5:c.319+2381G>A
NM_001163817.1:c.1372G>A	NP_001157289.1:p.Asp458Asn
NM_001360.2:c.1372G>A , LRG_340t1:c.1372G>A	NP_001351.2:p.Asp458Asn
XM_011544777.1:c.*135G>A	XP_011543079.1:n.*135G>A
XM_011544777.2:c.*135G>A	XP_011543079.1:n.*135G>A
NM_001163817.2:c.1372G>A	NP_001157289.1:p.Asp458Asn
NM_001360.3:c.1372G>A MANE Select	NP_001351.2:p.Asp458Asn