Canonical Allele Identifier: CA404321800

Gene: GCDH

Linked Data

• ClinVar Variation Id: 1426297
• ClinVar RCV Id: RCV001957618
• dbSNP Id: rs1432619357
• MyVariant Identifiers: chr19:g.13008645C>G (hg19) ; chr19:g.12897831C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12897831C>G , CM000681.2:g.12897831C>G	GRCh38
NC_000019.9:g.13008645C>G , CM000681.1:g.13008645C>G	GRCh37
NC_000019.8:g.12869645C>G	NCBI36
NG_009292.1:g.11672C>G
NG_033049.1:g.26442G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.1211C>G MANE Select	ENSP00000222214.4:p.Ala404Gly
ENST00000222214.9:c.1211C>G	ENSP00000222214.4:p.Ala404Gly
ENST00000585420.5:n.1541C>G
ENST00000590472.5:c.255C>G
ENST00000590530.5:c.*651C>G	ENSP00000468452.1:n.*651C>G
ENST00000591043.1:n.1521C>G
ENST00000591050.1:c.178C>G
ENST00000591470.5:c.1211C>G	ENSP00000466845.1:p.Ala404Gly
NM_000159.3:c.1211C>G	NP_000150.1:p.Ala404Gly
NM_013976.3:c.1211C>G	NP_039663.1:p.Ala404Gly
NR_102316.1:n.1374C>G
NR_102317.1:n.1592C>G
XM_006722721.2:c.1211C>G	XP_006722784.1:p.Ala404Gly
XM_011527899.1:c.1211C>G	XP_011526201.1:p.Ala404Gly
XM_011527900.1:c.1211C>G	XP_011526202.1:p.Ala404Gly
XM_011527899.2:c.1211C>G	XP_011526201.1:p.Ala404Gly
XM_011527900.2:c.1211C>G	XP_011526202.1:p.Ala404Gly
XM_017026580.1:c.1211C>G	XP_016882069.1:p.Ala404Gly
NM_000159.4:c.1211C>G MANE Select	NP_000150.1:p.Ala404Gly
NM_013976.4:c.1211C>G	NP_039663.1:p.Ala404Gly
NM_013976.5:c.1211C>G	NP_039663.1:p.Ala404Gly