Canonical Allele Identifier: CA505643408

Gene: GCDH

Linked Data

• MyVariant Identifiers: chr19:g.13004298A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12893484A>C , CM000681.2:g.12893484A>C	GRCh38
NC_000019.9:g.13004298A>C , CM000681.1:g.13004298A>C	GRCh37
NC_000019.8:g.12865298A>C	NCBI36
NG_009292.1:g.7325A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.336A>C MANE Select	ENSP00000222214.4:p.Gly112=
ENST00000222214.9:c.336A>C	ENSP00000222214.4:p.Gly112=
ENST00000421816.6:n.314A>C
ENST00000585420.5:n.701A>C
ENST00000587072.1:c.384A>C	ENSP00000468584.1:p.Gly128=
ENST00000587832.5:n.393A>C
ENST00000588905.5:c.300A>C	ENSP00000465770.1:p.Gly100=
ENST00000589039.5:c.273A>C	ENSP00000465618.1:p.Gly91=
ENST00000590530.5:c.391A>C	ENSP00000468452.1:p.Ile131Leu
ENST00000590627.5:n.701A>C
ENST00000591043.1:n.372A>C
ENST00000591470.5:c.336A>C	ENSP00000466845.1:p.Gly112=
NM_000159.3:c.336A>C	NP_000150.1:p.Gly112=
NM_013976.3:c.336A>C	NP_039663.1:p.Gly112=
NR_102316.1:n.499A>C
NR_102317.1:n.752A>C
XM_006722721.2:c.336A>C	XP_006722784.1:p.Gly112=
XM_011527899.1:c.336A>C	XP_011526201.1:p.Gly112=
XM_011527900.1:c.336A>C	XP_011526202.1:p.Gly112=
XM_011527899.2:c.336A>C	XP_011526201.1:p.Gly112=
XM_011527900.2:c.336A>C	XP_011526202.1:p.Gly112=
XM_017026580.1:c.336A>C	XP_016882069.1:p.Gly112=
NM_000159.4:c.336A>C MANE Select	NP_000150.1:p.Gly112=
NM_013976.4:c.336A>C	NP_039663.1:p.Gly112=
NM_013976.5:c.336A>C	NP_039663.1:p.Gly112=