Canonical Allele Identifier: CA475520143

Gene: DHCR7

Linked Data

• gnomAD v4: 11-71444023-G-C
• MyVariant Identifiers: chr11:g.71155069G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.71444023G>C , CM000673.2:g.71444023G>C	GRCh38
NC_000011.9:g.71155069G>C , CM000673.1:g.71155069G>C	GRCh37
NC_000011.8:g.70832717G>C	NCBI36
NG_012655.2:g.9409C>G , LRG_340:g.9409C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525346.6:c.291C>G	ENSP00000435707.3:p.Ala97=
ENST00000526780.6:c.291C>G	ENSP00000435668.2:p.Ala97=
ENST00000527316.6:c.117C>G	ENSP00000435047.2:p.Ala39=
ENST00000682708.1:c.291C>G	ENSP00000506866.1:p.Ala97=
ENST00000682880.1:c.291C>G	ENSP00000507520.1:p.Ala97=
ENST00000683287.1:c.291C>G	ENSP00000507607.1:p.Ala97=
ENST00000683714.1:c.291C>G	ENSP00000508207.1:p.Ala97=
ENST00000683874.1:n.568C>G
ENST00000685320.1:c.-295C>G	ENSP00000509319.1:n.-295C>G
ENST00000690257.1:c.195C>G	ENSP00000510750.1:p.Ala65=
ENST00000355527.8:c.291C>G MANE Select	ENSP00000347717.4:p.Ala97=
ENST00000355527.7:c.291C>G	ENSP00000347717.3:p.Ala97=
ENST00000407721.6:c.291C>G	ENSP00000384739.2:p.Ala97=
ENST00000525346.5:c.291C>G	ENSP00000435707.2:p.Ala97=
ENST00000526780.5:c.291C>G	ENSP00000435668.1:p.Ala97=
ENST00000527316.5:c.195C>G	ENSP00000435047.1:p.Ala65=
ENST00000531364.5:c.291C>G	ENSP00000432589.1:p.Ala97=
NM_001163817.1:c.291C>G	NP_001157289.1:p.Ala97=
NM_001360.2:c.291C>G , LRG_340t1:c.291C>G	NP_001351.2:p.Ala97=
XM_011544777.1:c.291C>G	XP_011543079.1:p.Ala97=
XM_011544777.2:c.291C>G	XP_011543079.1:p.Ala97=
NM_001163817.2:c.291C>G	NP_001157289.1:p.Ala97=
NM_001360.3:c.291C>G MANE Select	NP_001351.2:p.Ala97=