Canonical Allele Identifier: CA2323622085

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12893622G= , CM000681.2:g.12893622G=	GRCh38
NC_000019.9:g.13004436G= , CM000681.1:g.13004436G=	GRCh37
NC_000019.8:g.12865436G=	NCBI36
NG_009292.1:g.7463G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.474G= MANE Select	ENSP00000222214.4:p.Glu158=
ENST00000222214.9:c.474G=	ENSP00000222214.4:p.Glu158=
ENST00000421816.6:n.452G=
ENST00000585420.5:n.839G=
ENST00000587832.5:n.531G=
ENST00000588905.5:c.438G=	ENSP00000465770.1:p.Glu146=
ENST00000589039.5:c.411G=	ENSP00000465618.1:p.Glu137=
ENST00000590530.5:c.529G=	ENSP00000468452.1:p.Gly177=
ENST00000590627.5:n.839G=
ENST00000591043.1:n.510G=
ENST00000591470.5:c.474G=	ENSP00000466845.1:p.Glu158=
NM_000159.3:c.474G=	NP_000150.1:p.Glu158=
NM_013976.3:c.474G=	NP_039663.1:p.Glu158=
NR_102316.1:n.637G=
NR_102317.1:n.890G=
XM_006722721.2:c.474G=	XP_006722784.1:p.Glu158=
XM_011527899.1:c.474G=	XP_011526201.1:p.Glu158=
XM_011527900.1:c.474G=	XP_011526202.1:p.Glu158=
XM_011527899.2:c.474G=	XP_011526201.1:p.Glu158=
XM_011527900.2:c.474G=	XP_011526202.1:p.Glu158=
XM_017026580.1:c.474G=	XP_016882069.1:p.Glu158=
NM_000159.4:c.474G= MANE Select	NP_000150.1:p.Glu158=
NM_013976.4:c.474G=	NP_039663.1:p.Glu158=
NM_013976.5:c.474G=	NP_039663.1:p.Glu158=