Canonical Allele Identifier: CA9234391

Gene: GCDH

Linked Data

• dbSNP Id: rs751454561
• ExAC: 19:13004416 A / G
• gnomAD v2: 19-13004416-A-G
• gnomAD v4: 19-12893602-A-G
• MyVariant Identifiers: chr19:g.13004416A>G (hg19) ; chr19:g.12893602A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12893602A>G , CM000681.2:g.12893602A>G	GRCh38
NC_000019.9:g.13004416A>G , CM000681.1:g.13004416A>G	GRCh37
NC_000019.8:g.12865416A>G	NCBI36
NG_009292.1:g.7443A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.454A>G MANE Select	ENSP00000222214.4:p.Ile152Val
ENST00000222214.9:c.454A>G	ENSP00000222214.4:p.Ile152Val
ENST00000421816.6:n.432A>G
ENST00000585420.5:n.819A>G
ENST00000587832.5:n.511A>G
ENST00000588905.5:c.418A>G	ENSP00000465770.1:p.Ile140Val
ENST00000589039.5:c.391A>G	ENSP00000465618.1:p.Ile131Val
ENST00000590530.5:c.509A>G	ENSP00000468452.1:p.Tyr170Cys
ENST00000590627.5:n.819A>G
ENST00000591043.1:n.490A>G
ENST00000591470.5:c.454A>G	ENSP00000466845.1:p.Ile152Val
NM_000159.3:c.454A>G	NP_000150.1:p.Ile152Val
NM_013976.3:c.454A>G	NP_039663.1:p.Ile152Val
NR_102316.1:n.617A>G
NR_102317.1:n.870A>G
XM_006722721.2:c.454A>G	XP_006722784.1:p.Ile152Val
XM_011527899.1:c.454A>G	XP_011526201.1:p.Ile152Val
XM_011527900.1:c.454A>G	XP_011526202.1:p.Ile152Val
XM_011527899.2:c.454A>G	XP_011526201.1:p.Ile152Val
XM_011527900.2:c.454A>G	XP_011526202.1:p.Ile152Val
XM_017026580.1:c.454A>G	XP_016882069.1:p.Ile152Val
NM_000159.4:c.454A>G MANE Select	NP_000150.1:p.Ile152Val
NM_013976.4:c.454A>G	NP_039663.1:p.Ile152Val
NM_013976.5:c.454A>G	NP_039663.1:p.Ile152Val