Canonical Allele Identifier: CA6162322

Gene: DHCR7

Linked Data

• dbSNP Id: rs768526200
• ExAC: 11:71146778 C / A
• gnomAD v2: 11-71146778-C-A
• gnomAD v4: 11-71435732-C-A
• MyVariant Identifiers: chr11:g.71146778C>A (hg19) ; chr11:g.71435732C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435732C>A , CM000673.2:g.71435732C>A	GRCh38
NC_000011.9:g.71146778C>A , CM000673.1:g.71146778C>A	GRCh37
NC_000011.8:g.70824426C>A	NCBI36
NG_012655.2:g.17700G>T , LRG_340:g.17700G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525346.6:c.1071G>T	ENSP00000435707.3:p.Gln357His
ENST00000526780.6:c.1071G>T	ENSP00000435668.2:p.Gln357His
ENST00000527316.6:c.897G>T	ENSP00000435047.2:p.Gln299His
ENST00000682708.1:c.1122G>T	ENSP00000506866.1:p.Gln374His
ENST00000683287.1:c.1107G>T	ENSP00000507607.1:p.Gln369His
ENST00000683714.1:c.1079G>T	ENSP00000508207.1:p.Arg360Ile
ENST00000684396.1:n.1111G>T
ENST00000685320.1:c.486G>T	ENSP00000509319.1:p.Gln162His
ENST00000690257.1:c.975G>T	ENSP00000510750.1:p.Gln325His
ENST00000355527.8:c.1071G>T MANE Select	ENSP00000347717.4:p.Gln357His
ENST00000355527.7:c.1071G>T	ENSP00000347717.3:p.Gln357His
ENST00000407721.6:c.1071G>T	ENSP00000384739.2:p.Gln357His
ENST00000525137.1:c.572G>T	ENSP00000435956.1:p.Arg191Ile
ENST00000533800.5:c.321G>T	ENSP00000435011.1:p.Gln107His
ENST00000534795.5:c.319+2080G>T
NM_001163817.1:c.1071G>T	NP_001157289.1:p.Gln357His
NM_001360.2:c.1071G>T , LRG_340t1:c.1071G>T	NP_001351.2:p.Gln357His
XM_011544777.1:c.1205G>T	XP_011543079.1:p.Arg402Ile
XM_011544777.2:c.1205G>T	XP_011543079.1:p.Arg402Ile
NM_001163817.2:c.1071G>T	NP_001157289.1:p.Gln357His
NM_001360.3:c.1071G>T MANE Select	NP_001351.2:p.Gln357His