Canonical Allele Identifier: CA404318601

Gene: GCDH

Linked Data

• gnomAD v4: 19-12896251-T-C
• MyVariant Identifiers: chr19:g.13007065T>C (hg19) ; chr19:g.12896251T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896251T>C , CM000681.2:g.12896251T>C	GRCh38
NC_000019.9:g.13007065T>C , CM000681.1:g.13007065T>C	GRCh37
NC_000019.8:g.12868065T>C	NCBI36
NG_009292.1:g.10092T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.682T>C MANE Select	ENSP00000222214.4:p.Cys228Arg
ENST00000222214.9:c.682T>C	ENSP00000222214.4:p.Cys228Arg
ENST00000421816.6:n.660T>C
ENST00000585420.5:n.1012T>C
ENST00000590530.5:c.*122T>C	ENSP00000468452.1:n.*122T>C
ENST00000591043.1:n.718T>C
ENST00000591470.5:c.682T>C	ENSP00000466845.1:p.Cys228Arg
NM_000159.3:c.682T>C	NP_000150.1:p.Cys228Arg
NM_013976.3:c.682T>C	NP_039663.1:p.Cys228Arg
NR_102316.1:n.845T>C
NR_102317.1:n.1063T>C
XM_006722721.2:c.682T>C	XP_006722784.1:p.Cys228Arg
XM_011527899.1:c.682T>C	XP_011526201.1:p.Cys228Arg
XM_011527900.1:c.682T>C	XP_011526202.1:p.Cys228Arg
XM_011527899.2:c.682T>C	XP_011526201.1:p.Cys228Arg
XM_011527900.2:c.682T>C	XP_011526202.1:p.Cys228Arg
XM_017026580.1:c.682T>C	XP_016882069.1:p.Cys228Arg
NM_000159.4:c.682T>C MANE Select	NP_000150.1:p.Cys228Arg
NM_013976.4:c.682T>C	NP_039663.1:p.Cys228Arg
NM_013976.5:c.682T>C	NP_039663.1:p.Cys228Arg