Canonical Allele Identifier: CA2323621999

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12893487T= , CM000681.2:g.12893487T=	GRCh38
NC_000019.9:g.13004301T= , CM000681.1:g.13004301T=	GRCh37
NC_000019.8:g.12865301T=	NCBI36
NG_009292.1:g.7328T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000159.4:c.339T= MANE Select	NP_000150.1:p.Tyr113=
ENST00000222214.10:c.339T= MANE Select	ENSP00000222214.4:p.Tyr113=
NM_000159.3:c.339T=	NP_000150.1:p.Tyr113=
NM_013976.3:c.339T=	NP_039663.1:p.Tyr113=
NM_013976.4:c.339T=	NP_039663.1:p.Tyr113=
NM_013976.5:c.339T=	NP_039663.1:p.Tyr113=
NR_102316.1:n.502T=
NR_102317.1:n.755T=
ENST00000222214.9:c.339T=	ENSP00000222214.4:p.Tyr113=
ENST00000421816.6:n.317T=
ENST00000585420.5:n.704T=
ENST00000587072.1:c.387T=	ENSP00000468584.1:p.Tyr129=
ENST00000587832.5:n.396T=
ENST00000588905.5:c.303T=	ENSP00000465770.1:p.Tyr101=
ENST00000589039.5:c.276T=	ENSP00000465618.1:p.Tyr92=
ENST00000590530.5:c.394T=	ENSP00000468452.1:p.Trp132=
ENST00000590627.5:n.704T=
ENST00000591043.1:n.375T=
ENST00000591470.5:c.339T=	ENSP00000466845.1:p.Tyr113=
XM_006722721.2:c.339T=	XP_006722784.1:p.Tyr113=
XM_011527899.1:c.339T=	XP_011526201.1:p.Tyr113=
XM_011527899.2:c.339T=	XP_011526201.1:p.Tyr113=
XM_011527900.1:c.339T=	XP_011526202.1:p.Tyr113=
XM_011527900.2:c.339T=	XP_011526202.1:p.Tyr113=
XM_017026580.1:c.339T=	XP_016882069.1:p.Tyr113=