Canonical Allele Identifier: CA2323623249

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896111A= , CM000681.2:g.12896111A=	GRCh38
NC_000019.9:g.13006925A= , CM000681.1:g.13006925A=	GRCh37
NC_000019.8:g.12867925A=	NCBI36
NG_009292.1:g.9952A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.625A= MANE Select	ENSP00000222214.4:p.Thr209=
ENST00000222214.9:c.625A=	ENSP00000222214.4:p.Thr209=
ENST00000421816.6:n.603A=
ENST00000585420.5:n.990A=
ENST00000590530.5:c.*65A=	ENSP00000468452.1:n.*65A=
ENST00000591043.1:n.661A=
ENST00000591470.5:c.625A=	ENSP00000466845.1:p.Thr209=
NM_000159.3:c.625A=	NP_000150.1:p.Thr209=
NM_013976.3:c.625A=	NP_039663.1:p.Thr209=
NR_102316.1:n.788A=
NR_102317.1:n.1041A=
XM_006722721.2:c.625A=	XP_006722784.1:p.Thr209=
XM_011527899.1:c.625A=	XP_011526201.1:p.Thr209=
XM_011527900.1:c.625A=	XP_011526202.1:p.Thr209=
XM_011527899.2:c.625A=	XP_011526201.1:p.Thr209=
XM_011527900.2:c.625A=	XP_011526202.1:p.Thr209=
XM_017026580.1:c.625A=	XP_016882069.1:p.Thr209=
NM_000159.4:c.625A= MANE Select	NP_000150.1:p.Thr209=
NM_013976.4:c.625A=	NP_039663.1:p.Thr209=
NM_013976.5:c.625A=	NP_039663.1:p.Thr209=