Canonical Allele Identifier: CA505641337

Gene: GCDH

Linked Data

• ClinVar Variation Id: 1998366
• ClinVar RCV Id: RCV002810409
• MyVariant Identifiers: chr19:g.13002317A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12891503A>G , CM000681.2:g.12891503A>G	GRCh38
NC_000019.9:g.13002317A>G , CM000681.1:g.13002317A>G	GRCh37
NC_000019.8:g.12863317A>G	NCBI36
NG_009292.1:g.5344A>G
NG_013087.1:g.701T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.108A>G MANE Select	ENSP00000222214.4:p.Thr36=
ENST00000222214.9:c.108A>G	ENSP00000222214.4:p.Thr36=
ENST00000421816.6:n.168+108A>G
ENST00000585420.5:n.165A>G
ENST00000585760.5:n.144A>G
ENST00000587072.1:c.108A>G	ENSP00000468584.1:p.Thr36=
ENST00000587832.5:n.165A>G
ENST00000588905.5:c.91+108A>G	ENSP00000465770.1:n.91+108A>G
ENST00000589039.5:c.108A>G	ENSP00000465618.1:p.Thr36=
ENST00000590445.5:c.108A>G	ENSP00000468125.1:p.Thr36=
ENST00000590530.5:c.108A>G	ENSP00000468452.1:p.Thr36=
ENST00000590627.5:n.165A>G
ENST00000591043.1:n.144A>G
ENST00000591470.5:c.108A>G	ENSP00000466845.1:p.Thr36=
NM_000159.3:c.108A>G	NP_000150.1:p.Thr36=
NM_013976.3:c.108A>G	NP_039663.1:p.Thr36=
NR_102316.1:n.216A>G
NR_102317.1:n.216A>G
XM_006722721.2:c.108A>G	XP_006722784.1:p.Thr36=
XM_011527899.1:c.108A>G	XP_011526201.1:p.Thr36=
XM_011527900.1:c.108A>G	XP_011526202.1:p.Thr36=
XM_011527899.2:c.108A>G	XP_011526201.1:p.Thr36=
XM_011527900.2:c.108A>G	XP_011526202.1:p.Thr36=
XM_017026580.1:c.108A>G	XP_016882069.1:p.Thr36=
NM_000159.4:c.108A>G MANE Select	NP_000150.1:p.Thr36=
NM_013976.4:c.108A>G	NP_039663.1:p.Thr36=
NM_013976.5:c.108A>G	NP_039663.1:p.Thr36=