Canonical Allele Identifier: CA475860932

Gene: DHCR7

Linked Data

• dbSNP Id: rs1949266143
• gnomAD v4: 11-71435501-G-A
• MyVariant Identifiers: chr11:g.71146547G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435501G>A , CM000673.2:g.71435501G>A	GRCh38
NC_000011.9:g.71146547G>A , CM000673.1:g.71146547G>A	GRCh37
NC_000011.8:g.70824195G>A	NCBI36
NG_012655.2:g.17931C>T , LRG_340:g.17931C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1302C>T	ENSP00000435707.3:p.Ile434=
ENST00000526780.6:c.1302C>T	ENSP00000435668.2:p.Ile434=
ENST00000527316.6:c.1128C>T	ENSP00000435047.2:p.Ile376=
ENST00000682708.1:c.1353C>T	ENSP00000506866.1:p.Ile451=
ENST00000683287.1:c.1338C>T	ENSP00000507607.1:p.Ile446=
ENST00000683714.1:c.*65C>T	ENSP00000508207.1:n.*65C>T
ENST00000684396.1:n.1342C>T
ENST00000685320.1:c.717C>T	ENSP00000509319.1:p.Ile239=
ENST00000690257.1:c.1206C>T	ENSP00000510750.1:p.Ile402=
ENST00000355527.8:c.1302C>T MANE Select	ENSP00000347717.4:p.Ile434=
ENST00000355527.7:c.1302C>T	ENSP00000347717.3:p.Ile434=
ENST00000407721.6:c.1302C>T	ENSP00000384739.2:p.Ile434=
ENST00000525137.1:c.803C>T	ENSP00000435956.1:n.803C>T
ENST00000533800.5:c.552C>T	ENSP00000435011.1:p.Ile184=
ENST00000534795.5:c.319+2311C>T
NM_001163817.1:c.1302C>T	NP_001157289.1:p.Ile434=
NM_001360.2:c.1302C>T , LRG_340t1:c.1302C>T	NP_001351.2:p.Ile434=
XM_011544777.1:c.*65C>T	XP_011543079.1:n.*65C>T
XM_011544777.2:c.*65C>T	XP_011543079.1:n.*65C>T
NM_001163817.2:c.1302C>T	NP_001157289.1:p.Ile434=
NM_001360.3:c.1302C>T MANE Select	NP_001351.2:p.Ile434=