Canonical Allele Identifier: CA2323622095

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12893635A= , CM000681.2:g.12893635A=	GRCh38
NC_000019.9:g.13004449A= , CM000681.1:g.13004449A=	GRCh37
NC_000019.8:g.12865449A=	NCBI36
NG_009292.1:g.7476A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.487A= MANE Select	ENSP00000222214.4:p.Lys163=
ENST00000222214.9:c.487A=	ENSP00000222214.4:p.Lys163=
ENST00000421816.6:n.465A=
ENST00000585420.5:n.852A=
ENST00000587832.5:n.544A=
ENST00000588905.5:c.451A=	ENSP00000465770.1:p.Lys151=
ENST00000589039.5:c.424A=	ENSP00000465618.1:p.Lys142=
ENST00000590530.5:c.542A=	ENSP00000468452.1:p.Glu181=
ENST00000590627.5:n.852A=
ENST00000591043.1:n.523A=
ENST00000591470.5:c.487A=	ENSP00000466845.1:p.Lys163=
NM_000159.3:c.487A=	NP_000150.1:p.Lys163=
NM_013976.3:c.487A=	NP_039663.1:p.Lys163=
NR_102316.1:n.650A=
NR_102317.1:n.903A=
XM_006722721.2:c.487A=	XP_006722784.1:p.Lys163=
XM_011527899.1:c.487A=	XP_011526201.1:p.Lys163=
XM_011527900.1:c.487A=	XP_011526202.1:p.Lys163=
XM_011527899.2:c.487A=	XP_011526201.1:p.Lys163=
XM_011527900.2:c.487A=	XP_011526202.1:p.Lys163=
XM_017026580.1:c.487A=	XP_016882069.1:p.Lys163=
NM_000159.4:c.487A= MANE Select	NP_000150.1:p.Lys163=
NM_013976.4:c.487A=	NP_039663.1:p.Lys163=
NM_013976.5:c.487A=	NP_039663.1:p.Lys163=