Canonical Allele Identifier: CA2323623188

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896001A= , CM000681.2:g.12896001A=	GRCh38
NC_000019.9:g.13006815A= , CM000681.1:g.13006815A=	GRCh37
NC_000019.8:g.12867815A=	NCBI36
NG_009292.1:g.9842A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.515A= MANE Select	ENSP00000222214.4:p.Glu172=
ENST00000222214.9:c.515A=	ENSP00000222214.4:p.Glu172=
ENST00000421816.6:n.493A=
ENST00000585420.5:n.880A=
ENST00000588905.5:c.479A=	ENSP00000465770.1:p.Glu160=
ENST00000590530.5:c.570A=	ENSP00000468452.1:p.Gly190=
ENST00000591043.1:n.551A=
ENST00000591470.5:c.515A=	ENSP00000466845.1:p.Glu172=
NM_000159.3:c.515A=	NP_000150.1:p.Glu172=
NM_013976.3:c.515A=	NP_039663.1:p.Glu172=
NR_102316.1:n.678A=
NR_102317.1:n.931A=
XM_006722721.2:c.515A=	XP_006722784.1:p.Glu172=
XM_011527899.1:c.515A=	XP_011526201.1:p.Glu172=
XM_011527900.1:c.515A=	XP_011526202.1:p.Glu172=
XM_011527899.2:c.515A=	XP_011526201.1:p.Glu172=
XM_011527900.2:c.515A=	XP_011526202.1:p.Glu172=
XM_017026580.1:c.515A=	XP_016882069.1:p.Glu172=
NM_000159.4:c.515A= MANE Select	NP_000150.1:p.Glu172=
NM_013976.4:c.515A=	NP_039663.1:p.Glu172=
NM_013976.5:c.515A=	NP_039663.1:p.Glu172=