Canonical Allele Identifier: CA2695228355

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12897830dup , CM000681.2:g.12897830dup	GRCh38
NC_000019.9:g.13008644dup , CM000681.1:g.13008644dup	GRCh37
NC_000019.8:g.12869644dup	NCBI36
NG_009292.1:g.11671dup
NG_033049.1:g.26443dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000222214.10:c.1210dup MANE Select	ENSP00000222214.4:p.Ala404GlyfsTer15
ENST00000222214.9:c.1210dup	ENSP00000222214.4:p.Ala404GlyfsTer15
ENST00000585420.5:n.1540dup
ENST00000590472.5:c.254dup
ENST00000590530.5:c.*650dup	ENSP00000468452.1:n.*650dup
ENST00000591043.1:n.1520dup
ENST00000591050.1:c.177dup
ENST00000591470.5:c.1210dup	ENSP00000466845.1:p.Ala404GlyfsTer15
NM_000159.3:c.1210dup	NP_000150.1:p.Ala404GlyfsTer15
NM_013976.3:c.1210dup	NP_039663.1:p.Ala404GlyfsTer?
NR_102316.1:n.1373dup
NR_102317.1:n.1591dup
XM_006722721.2:c.1210dup	XP_006722784.1:p.Ala404GlyfsTer?
XM_011527899.1:c.1210dup	XP_011526201.1:p.Ala404GlyfsTer13
XM_011527900.1:c.1210dup	XP_011526202.1:p.Ala404GlyfsTer?
XM_011527899.2:c.1210dup	XP_011526201.1:p.Ala404GlyfsTer13
XM_011527900.2:c.1210dup	XP_011526202.1:p.Ala404GlyfsTer?
XM_017026580.1:c.1210dup	XP_016882069.1:p.Ala404GlyfsTer?
NM_000159.4:c.1210dup MANE Select	NP_000150.1:p.Ala404GlyfsTer15
NM_013976.4:c.1210dup	NP_039663.1:p.Ala404GlyfsTer?
NM_013976.5:c.1210dup	NP_039663.1:p.Ala404GlyfsTer?