Canonical Allele Identifier: CA2323623664

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896951G= , CM000681.2:g.12896951G=	GRCh38
NC_000019.9:g.13007765G= , CM000681.1:g.13007765G=	GRCh37
NC_000019.8:g.12868765G=	NCBI36
NG_009292.1:g.10792G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.894G= MANE Select	ENSP00000222214.4:p.Ala298=
ENST00000222214.9:c.894G=	ENSP00000222214.4:p.Ala298=
ENST00000421816.6:n.872G=
ENST00000585420.5:n.1224G=
ENST00000590530.5:c.*334G=	ENSP00000468452.1:n.*334G=
ENST00000591043.1:n.930G=
ENST00000591470.5:c.894G=	ENSP00000466845.1:p.Ala298=
NM_000159.3:c.894G=	NP_000150.1:p.Ala298=
NM_013976.3:c.894G=	NP_039663.1:p.Ala298=
NR_102316.1:n.1057G=
NR_102317.1:n.1275G=
XM_006722721.2:c.894G=	XP_006722784.1:p.Ala298=
XM_011527899.1:c.894G=	XP_011526201.1:p.Ala298=
XM_011527900.1:c.894G=	XP_011526202.1:p.Ala298=
XM_011527899.2:c.894G=	XP_011526201.1:p.Ala298=
XM_011527900.2:c.894G=	XP_011526202.1:p.Ala298=
XM_017026580.1:c.894G=	XP_016882069.1:p.Ala298=
NM_000159.4:c.894G= MANE Select	NP_000150.1:p.Ala298=
NM_013976.4:c.894G=	NP_039663.1:p.Ala298=
NM_013976.5:c.894G=	NP_039663.1:p.Ala298=