Canonical Allele Identifier: CA505644685

Gene: GCDH

Linked Data

• MyVariant Identifiers: chr19:g.13004430C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12893616C>A , CM000681.2:g.12893616C>A	GRCh38
NC_000019.9:g.13004430C>A , CM000681.1:g.13004430C>A	GRCh37
NC_000019.8:g.12865430C>A	NCBI36
NG_009292.1:g.7457C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.468C>A MANE Select	ENSP00000222214.4:p.Gly156=
ENST00000222214.9:c.468C>A	ENSP00000222214.4:p.Gly156=
ENST00000421816.6:n.446C>A
ENST00000585420.5:n.833C>A
ENST00000587832.5:n.525C>A
ENST00000588905.5:c.432C>A	ENSP00000465770.1:p.Gly144=
ENST00000589039.5:c.405C>A	ENSP00000465618.1:p.Gly135=
ENST00000590530.5:c.523C>A	ENSP00000468452.1:p.Gln175Lys
ENST00000590627.5:n.833C>A
ENST00000591043.1:n.504C>A
ENST00000591470.5:c.468C>A	ENSP00000466845.1:p.Gly156=
NM_000159.3:c.468C>A	NP_000150.1:p.Gly156=
NM_013976.3:c.468C>A	NP_039663.1:p.Gly156=
NR_102316.1:n.631C>A
NR_102317.1:n.884C>A
XM_006722721.2:c.468C>A	XP_006722784.1:p.Gly156=
XM_011527899.1:c.468C>A	XP_011526201.1:p.Gly156=
XM_011527900.1:c.468C>A	XP_011526202.1:p.Gly156=
XM_011527899.2:c.468C>A	XP_011526201.1:p.Gly156=
XM_011527900.2:c.468C>A	XP_011526202.1:p.Gly156=
XM_017026580.1:c.468C>A	XP_016882069.1:p.Gly156=
NM_000159.4:c.468C>A MANE Select	NP_000150.1:p.Gly156=
NM_013976.4:c.468C>A	NP_039663.1:p.Gly156=
NM_013976.5:c.468C>A	NP_039663.1:p.Gly156=