Canonical Allele Identifier: CA404319358

Gene: GCDH

Linked Data

• ClinVar Variation Id: 2864675
• ClinVar RCV Id: RCV003602591
• MyVariant Identifiers: chr19:g.13007749C>T (hg19) ; chr19:g.12896935C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896935C>T , CM000681.2:g.12896935C>T	GRCh38
NC_000019.9:g.13007749C>T , CM000681.1:g.13007749C>T	GRCh37
NC_000019.8:g.12868749C>T	NCBI36
NG_009292.1:g.10776C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.878C>T MANE Select	ENSP00000222214.4:p.Ala293Val
ENST00000222214.9:c.878C>T	ENSP00000222214.4:p.Ala293Val
ENST00000421816.6:n.856C>T
ENST00000585420.5:n.1208C>T
ENST00000590530.5:c.*318C>T	ENSP00000468452.1:n.*318C>T
ENST00000591043.1:n.914C>T
ENST00000591470.5:c.878C>T	ENSP00000466845.1:p.Ala293Val
NM_000159.3:c.878C>T	NP_000150.1:p.Ala293Val
NM_013976.3:c.878C>T	NP_039663.1:p.Ala293Val
NR_102316.1:n.1041C>T
NR_102317.1:n.1259C>T
XM_006722721.2:c.878C>T	XP_006722784.1:p.Ala293Val
XM_011527899.1:c.878C>T	XP_011526201.1:p.Ala293Val
XM_011527900.1:c.878C>T	XP_011526202.1:p.Ala293Val
XM_011527899.2:c.878C>T	XP_011526201.1:p.Ala293Val
XM_011527900.2:c.878C>T	XP_011526202.1:p.Ala293Val
XM_017026580.1:c.878C>T	XP_016882069.1:p.Ala293Val
NM_000159.4:c.878C>T MANE Select	NP_000150.1:p.Ala293Val
NM_013976.4:c.878C>T	NP_039663.1:p.Ala293Val
NM_013976.5:c.878C>T	NP_039663.1:p.Ala293Val