Canonical Allele Identifier: CA2323623377

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896355C= , CM000681.2:g.12896355C=	GRCh38
NC_000019.9:g.13007169C= , CM000681.1:g.13007169C=	GRCh37
NC_000019.8:g.12868169C=	NCBI36
NG_009292.1:g.10196C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.786C= MANE Select	ENSP00000222214.4:p.Gly262=
ENST00000222214.9:c.786C=	ENSP00000222214.4:p.Gly262=
ENST00000421816.6:n.764C=
ENST00000585420.5:n.1116C=
ENST00000590530.5:c.*226C=	ENSP00000468452.1:n.*226C=
ENST00000591043.1:n.822C=
ENST00000591470.5:c.786C=	ENSP00000466845.1:p.Gly262=
NM_000159.3:c.786C=	NP_000150.1:p.Gly262=
NM_013976.3:c.786C=	NP_039663.1:p.Gly262=
NR_102316.1:n.949C=
NR_102317.1:n.1167C=
XM_006722721.2:c.786C=	XP_006722784.1:p.Gly262=
XM_011527899.1:c.786C=	XP_011526201.1:p.Gly262=
XM_011527900.1:c.786C=	XP_011526202.1:p.Gly262=
XM_011527899.2:c.786C=	XP_011526201.1:p.Gly262=
XM_011527900.2:c.786C=	XP_011526202.1:p.Gly262=
XM_017026580.1:c.786C=	XP_016882069.1:p.Gly262=
NM_000159.4:c.786C= MANE Select	NP_000150.1:p.Gly262=
NM_013976.4:c.786C=	NP_039663.1:p.Gly262=
NM_013976.5:c.786C=	NP_039663.1:p.Gly262=