Canonical Allele Identifier: CA9234207

Gene: GCDH

Linked Data

• ClinVar Variation Id: 1313580
• ClinVar RCV Id: RCV001763944
• dbSNP Id: rs759599442
• ExAC: 19:13002319 A / G
• gnomAD v2: 19-13002319-A-G
• gnomAD v3: 19-12891505-A-G
• gnomAD v4: 19-12891505-A-G
• MyVariant Identifiers: chr19:g.13002319A>G (hg19) ; chr19:g.12891505A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12891505A>G , CM000681.2:g.12891505A>G	GRCh38
NC_000019.9:g.13002319A>G , CM000681.1:g.13002319A>G	GRCh37
NC_000019.8:g.12863319A>G	NCBI36
NG_009292.1:g.5346A>G
NG_013087.1:g.699T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.110A>G MANE Select	ENSP00000222214.4:p.Gln37Arg
ENST00000222214.9:c.110A>G	ENSP00000222214.4:p.Gln37Arg
ENST00000421816.6:n.168+110A>G
ENST00000585420.5:n.167A>G
ENST00000585760.5:n.146A>G
ENST00000587072.1:c.110A>G	ENSP00000468584.1:p.Gln37Arg
ENST00000587832.5:n.167A>G
ENST00000588905.5:c.91+110A>G	ENSP00000465770.1:n.91+110A>G
ENST00000589039.5:c.110A>G	ENSP00000465618.1:p.Gln37Arg
ENST00000590445.5:c.110A>G	ENSP00000468125.1:p.Gln37Arg
ENST00000590530.5:c.110A>G	ENSP00000468452.1:p.Gln37Arg
ENST00000590627.5:n.167A>G
ENST00000591043.1:n.146A>G
ENST00000591470.5:c.110A>G	ENSP00000466845.1:p.Gln37Arg
NM_000159.3:c.110A>G	NP_000150.1:p.Gln37Arg
NM_013976.3:c.110A>G	NP_039663.1:p.Gln37Arg
NR_102316.1:n.218A>G
NR_102317.1:n.218A>G
XM_006722721.2:c.110A>G	XP_006722784.1:p.Gln37Arg
XM_011527899.1:c.110A>G	XP_011526201.1:p.Gln37Arg
XM_011527900.1:c.110A>G	XP_011526202.1:p.Gln37Arg
XM_011527899.2:c.110A>G	XP_011526201.1:p.Gln37Arg
XM_011527900.2:c.110A>G	XP_011526202.1:p.Gln37Arg
XM_017026580.1:c.110A>G	XP_016882069.1:p.Gln37Arg
NM_000159.4:c.110A>G MANE Select	NP_000150.1:p.Gln37Arg
NM_013976.4:c.110A>G	NP_039663.1:p.Gln37Arg
NM_013976.5:c.110A>G	NP_039663.1:p.Gln37Arg