Canonical Allele Identifier: CA2323624169

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12897929G= , CM000681.2:g.12897929G=	GRCh38
NC_000019.9:g.13008743G= , CM000681.1:g.13008743G=	GRCh37
NC_000019.8:g.12869743G=	NCBI36
NG_009292.1:g.11770G=
NG_033049.1:g.26344C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.1243+66G= MANE Select	ENSP00000222214.4:n.1243+66G=
ENST00000222214.9:c.1243+66G=	ENSP00000222214.4:n.1243+66G=
ENST00000585420.5:n.1573+66G=
ENST00000590472.5:c.287+66G=
ENST00000590530.5:c.*683+66G=	ENSP00000468452.1:n.*683+66G=
ENST00000591043.1:n.1553+66G=
ENST00000591050.1:c.210+66G=
ENST00000591470.5:c.1243+66G=	ENSP00000466845.1:n.1243+66G=
NM_000159.3:c.1243+66G=	NP_000150.1:n.1243+66G=
NM_013976.3:c.1243+66G=	NP_039663.1:n.1243+66G=
NR_102316.1:n.1406+66G=
NR_102317.1:n.1624+66G=
XM_006722721.2:c.1243+66G=	XP_006722784.1:n.1243+66G=
XM_011527899.1:c.1243+66G=	XP_011526201.1:n.1243+66G=
XM_011527900.1:c.1243+66G=	XP_011526202.1:n.1243+66G=
XM_011527899.2:c.1243+66G=	XP_011526201.1:n.1243+66G=
XM_011527900.2:c.1243+66G=	XP_011526202.1:n.1243+66G=
XM_017026580.1:c.1243+66G=	XP_016882069.1:n.1243+66G=
NM_000159.4:c.1243+66G= MANE Select	NP_000150.1:n.1243+66G=
NM_013976.4:c.1243+66G=	NP_039663.1:n.1243+66G=
NM_013976.5:c.1243+66G=	NP_039663.1:n.1243+66G=