Canonical Allele Identifier: CA2323623268
Gene: GCDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12896155A= , CM000681.2:g.12896155A= GRCh38
NC_000019.9:g.13006969A= , CM000681.1:g.13006969A= GRCh37
NC_000019.8:g.12867969A= NCBI36
NG_009292.1:g.9996A=

Transcript Alleles

HGVS Amino-acid change
ENST00000222214.10:c.635+34A= MANE Select ENSP00000222214.4:n.635+34A=
ENST00000222214.9:c.635+34A= ENSP00000222214.4:n.635+34A=
ENST00000421816.6:n.613+34A=
ENST00000585420.5:n.1000+34A=
ENST00000590530.5:c.*75+34A= ENSP00000468452.1:n.*75+34A=
ENST00000591043.1:n.671+34A=
ENST00000591470.5:c.635+34A= ENSP00000466845.1:n.635+34A=
NM_000159.3:c.635+34A= NP_000150.1:n.635+34A=
NM_013976.3:c.635+34A= NP_039663.1:n.635+34A=
NR_102316.1:n.798+34A=
NR_102317.1:n.1051+34A=
XM_006722721.2:c.635+34A= XP_006722784.1:n.635+34A=
XM_011527899.1:c.635+34A= XP_011526201.1:n.635+34A=
XM_011527900.1:c.635+34A= XP_011526202.1:n.635+34A=
XM_011527899.2:c.635+34A= XP_011526201.1:n.635+34A=
XM_011527900.2:c.635+34A= XP_011526202.1:n.635+34A=
XM_017026580.1:c.635+34A= XP_016882069.1:n.635+34A=
NM_000159.4:c.635+34A= MANE Select NP_000150.1:n.635+34A=
NM_013976.4:c.635+34A= NP_039663.1:n.635+34A=
NM_013976.5:c.635+34A= NP_039663.1:n.635+34A=