Canonical Allele Identifier: CA2323624114

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12897833A= , CM000681.2:g.12897833A=	GRCh38
NC_000019.9:g.13008647A= , CM000681.1:g.13008647A=	GRCh37
NC_000019.8:g.12869647A=	NCBI36
NG_009292.1:g.11674A=
NG_033049.1:g.26440T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.1213A= MANE Select	ENSP00000222214.4:p.Met405=
ENST00000222214.9:c.1213A=	ENSP00000222214.4:p.Met405=
ENST00000585420.5:n.1543A=
ENST00000590472.5:c.257A=
ENST00000590530.5:c.*653A=	ENSP00000468452.1:n.*653A=
ENST00000591043.1:n.1523A=
ENST00000591050.1:c.180A=
ENST00000591470.5:c.1213A=	ENSP00000466845.1:p.Met405=
NM_000159.3:c.1213A=	NP_000150.1:p.Met405=
NM_013976.3:c.1213A=	NP_039663.1:p.Met405=
NR_102316.1:n.1376A=
NR_102317.1:n.1594A=
XM_006722721.2:c.1213A=	XP_006722784.1:p.Met405=
XM_011527899.1:c.1213A=	XP_011526201.1:p.Met405=
XM_011527900.1:c.1213A=	XP_011526202.1:p.Met405=
XM_011527899.2:c.1213A=	XP_011526201.1:p.Met405=
XM_011527900.2:c.1213A=	XP_011526202.1:p.Met405=
XM_017026580.1:c.1213A=	XP_016882069.1:p.Met405=
NM_000159.4:c.1213A= MANE Select	NP_000150.1:p.Met405=
NM_013976.4:c.1213A=	NP_039663.1:p.Met405=
NM_013976.5:c.1213A=	NP_039663.1:p.Met405=