Canonical Allele Identifier: CA2323624102

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12897815C= , CM000681.2:g.12897815C=	GRCh38
NC_000019.9:g.13008629C= , CM000681.1:g.13008629C=	GRCh37
NC_000019.8:g.12869629C=	NCBI36
NG_009292.1:g.11656C=
NG_033049.1:g.26458G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.1195C= MANE Select	ENSP00000222214.4:p.His399=
ENST00000222214.9:c.1195C=	ENSP00000222214.4:p.His399=
ENST00000585420.5:n.1525C=
ENST00000590472.5:c.239C=
ENST00000590530.5:c.*635C=	ENSP00000468452.1:n.*635C=
ENST00000591043.1:n.1505C=
ENST00000591050.1:c.162C=
ENST00000591470.5:c.1195C=	ENSP00000466845.1:p.His399=
NM_000159.3:c.1195C=	NP_000150.1:p.His399=
NM_013976.3:c.1195C=	NP_039663.1:p.His399=
NR_102316.1:n.1358C=
NR_102317.1:n.1576C=
XM_006722721.2:c.1195C=	XP_006722784.1:p.His399=
XM_011527899.1:c.1195C=	XP_011526201.1:p.His399=
XM_011527900.1:c.1195C=	XP_011526202.1:p.His399=
XM_011527899.2:c.1195C=	XP_011526201.1:p.His399=
XM_011527900.2:c.1195C=	XP_011526202.1:p.His399=
XM_017026580.1:c.1195C=	XP_016882069.1:p.His399=
NM_000159.4:c.1195C= MANE Select	NP_000150.1:p.His399=
NM_013976.4:c.1195C=	NP_039663.1:p.His399=
NM_013976.5:c.1195C=	NP_039663.1:p.His399=