Canonical Allele Identifier: CA10581471

Gene: GCDH

Linked Data

• ClinVar Variation Id: 235857
• ClinVar RCV Id: RCV000224005
• dbSNP Id: rs878853153
• MyVariant Identifiers: chr19:g.13004418C>G (hg19) ; chr19:g.12893604C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12893604C>G , CM000681.2:g.12893604C>G	GRCh38
NC_000019.9:g.13004418C>G , CM000681.1:g.13004418C>G	GRCh37
NC_000019.8:g.12865418C>G	NCBI36
NG_009292.1:g.7445C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.456C>G MANE Select	ENSP00000222214.4:p.Ile152Met
ENST00000222214.9:c.456C>G	ENSP00000222214.4:p.Ile152Met
ENST00000421816.6:n.434C>G
ENST00000585420.5:n.821C>G
ENST00000587832.5:n.513C>G
ENST00000588905.5:c.420C>G	ENSP00000465770.1:p.Ile140Met
ENST00000589039.5:c.393C>G	ENSP00000465618.1:p.Ile131Met
ENST00000590530.5:c.511C>G	ENSP00000468452.1:p.Leu171Val
ENST00000590627.5:n.821C>G
ENST00000591043.1:n.492C>G
ENST00000591470.5:c.456C>G	ENSP00000466845.1:p.Ile152Met
NM_000159.3:c.456C>G	NP_000150.1:p.Ile152Met
NM_013976.3:c.456C>G	NP_039663.1:p.Ile152Met
NR_102316.1:n.619C>G
NR_102317.1:n.872C>G
XM_006722721.2:c.456C>G	XP_006722784.1:p.Ile152Met
XM_011527899.1:c.456C>G	XP_011526201.1:p.Ile152Met
XM_011527900.1:c.456C>G	XP_011526202.1:p.Ile152Met
XM_011527899.2:c.456C>G	XP_011526201.1:p.Ile152Met
XM_011527900.2:c.456C>G	XP_011526202.1:p.Ile152Met
XM_017026580.1:c.456C>G	XP_016882069.1:p.Ile152Met
NM_000159.4:c.456C>G MANE Select	NP_000150.1:p.Ile152Met
NM_013976.4:c.456C>G	NP_039663.1:p.Ile152Met
NM_013976.5:c.456C>G	NP_039663.1:p.Ile152Met