Canonical Allele Identifier: CA645607005
Gene: GCDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12896000dup , CM000681.2:g.12896000dup GRCh38
NC_000019.9:g.13006814dup , CM000681.1:g.13006814dup GRCh37
NC_000019.8:g.12867814dup NCBI36
NG_009292.1:g.9841dup

Transcript Alleles

HGVS Amino-acid change
ENST00000222214.10:c.514dup MANE Select ENSP00000222214.4:p.Glu172GlyfsTer16
ENST00000222214.9:c.514dup ENSP00000222214.4:p.Glu172GlyfsTer16
ENST00000421816.6:n.492dup
ENST00000585420.5:n.879dup
ENST00000588905.5:c.478dup ENSP00000465770.1:p.Glu160GlyfsTer?
ENST00000590530.5:c.569dup ENSP00000468452.1:p.Ala191SerfsTer?
ENST00000591043.1:n.550dup
ENST00000591470.5:c.514dup ENSP00000466845.1:p.Glu172GlyfsTer16
NM_000159.3:c.514dup NP_000150.1:p.Glu172GlyfsTer16
NM_013976.3:c.514dup NP_039663.1:p.Glu172GlyfsTer16
NR_102316.1:n.677dup
NR_102317.1:n.930dup
XM_006722721.2:c.514dup XP_006722784.1:p.Glu172GlyfsTer16
XM_011527899.1:c.514dup XP_011526201.1:p.Glu172GlyfsTer16
XM_011527900.1:c.514dup XP_011526202.1:p.Glu172GlyfsTer16
XM_011527899.2:c.514dup XP_011526201.1:p.Glu172GlyfsTer16
XM_011527900.2:c.514dup XP_011526202.1:p.Glu172GlyfsTer16
XM_017026580.1:c.514dup XP_016882069.1:p.Glu172GlyfsTer16
NM_000159.4:c.514dup MANE Select NP_000150.1:p.Glu172GlyfsTer16
NM_013976.4:c.514dup NP_039663.1:p.Glu172GlyfsTer16
NM_013976.5:c.514dup NP_039663.1:p.Glu172GlyfsTer16