Canonical Allele Identifier: CA2576639209

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12893500del , CM000681.2:g.12893500del	GRCh38
NC_000019.9:g.13004314del , CM000681.1:g.13004314del	GRCh37
NC_000019.8:g.12865314del	NCBI36
NG_009292.1:g.7341del

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.352del MANE Select	ENSP00000222214.4:p.Val118PhefsTer24
ENST00000222214.9:c.352del	ENSP00000222214.4:p.Val118PhefsTer24
ENST00000421816.6:n.330del
ENST00000585420.5:n.717del
ENST00000587832.5:n.409del
ENST00000588905.5:c.316del	ENSP00000465770.1:p.Val106PhefsTer24
ENST00000589039.5:c.289del	ENSP00000465618.1:p.Val97PhefsTer24
ENST00000590530.5:c.407del	ENSP00000468452.1:p.Gly136ValfsTer?
ENST00000590627.5:n.717del
ENST00000591043.1:n.388del
ENST00000591470.5:c.352del	ENSP00000466845.1:p.Val118PhefsTer24
NM_000159.3:c.352del	NP_000150.1:p.Val118PhefsTer24
NM_013976.3:c.352del	NP_039663.1:p.Val118PhefsTer24
NR_102316.1:n.515del
NR_102317.1:n.768del
XM_006722721.2:c.352del	XP_006722784.1:p.Val118PhefsTer24
XM_011527899.1:c.352del	XP_011526201.1:p.Val118PhefsTer24
XM_011527900.1:c.352del	XP_011526202.1:p.Val118PhefsTer24
XM_011527899.2:c.352del	XP_011526201.1:p.Val118PhefsTer24
XM_011527900.2:c.352del	XP_011526202.1:p.Val118PhefsTer24
XM_017026580.1:c.352del	XP_016882069.1:p.Val118PhefsTer24
NM_000159.4:c.352del MANE Select	NP_000150.1:p.Val118PhefsTer24
NM_013976.4:c.352del	NP_039663.1:p.Val118PhefsTer24
NM_013976.5:c.352del	NP_039663.1:p.Val118PhefsTer24