Canonical Allele Identifier: CA381702023

Gene: DHCR7

Linked Data

• MyVariant Identifiers: chr11:g.71146744G>T (hg19) ; chr11:g.71435698G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71435698G>T , CM000673.2:g.71435698G>T	GRCh38
NC_000011.9:g.71146744G>T , CM000673.1:g.71146744G>T	GRCh37
NC_000011.8:g.70824392G>T	NCBI36
NG_012655.2:g.17734C>A , LRG_340:g.17734C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525346.6:c.1105C>A	ENSP00000435707.3:p.Leu369Ile
ENST00000526780.6:c.1105C>A	ENSP00000435668.2:p.Leu369Ile
ENST00000527316.6:c.931C>A	ENSP00000435047.2:p.Leu311Ile
ENST00000682708.1:c.1156C>A	ENSP00000506866.1:p.Leu386Ile
ENST00000683287.1:c.1141C>A	ENSP00000507607.1:p.Leu381Ile
ENST00000683714.1:c.1113C>A	ENSP00000508207.1:p.Ala371=
ENST00000684396.1:n.1145C>A
ENST00000685320.1:c.520C>A	ENSP00000509319.1:p.Leu174Ile
ENST00000690257.1:c.1009C>A	ENSP00000510750.1:p.Leu337Ile
ENST00000355527.8:c.1105C>A MANE Select	ENSP00000347717.4:p.Leu369Ile
ENST00000355527.7:c.1105C>A	ENSP00000347717.3:p.Leu369Ile
ENST00000407721.6:c.1105C>A	ENSP00000384739.2:p.Leu369Ile
ENST00000525137.1:c.606C>A	ENSP00000435956.1:p.Ala202=
ENST00000533800.5:c.355C>A	ENSP00000435011.1:p.Leu119Ile
ENST00000534795.5:c.319+2114C>A
NM_001163817.1:c.1105C>A	NP_001157289.1:p.Leu369Ile
NM_001360.2:c.1105C>A , LRG_340t1:c.1105C>A	NP_001351.2:p.Leu369Ile
XM_011544777.1:c.1239C>A	XP_011543079.1:p.Ala413=
XM_011544777.2:c.1239C>A	XP_011543079.1:p.Ala413=
NM_001163817.2:c.1105C>A	NP_001157289.1:p.Leu369Ile
NM_001360.3:c.1105C>A MANE Select	NP_001351.2:p.Leu369Ile