Canonical Allele Identifier: CA2323623279
Gene: GCDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12896170C= , CM000681.2:g.12896170C= GRCh38
NC_000019.9:g.13006984C= , CM000681.1:g.13006984C= GRCh37
NC_000019.8:g.12867984C= NCBI36
NG_009292.1:g.10011C=

Transcript Alleles

HGVS Amino-acid change
ENST00000222214.10:c.636-35C= MANE Select ENSP00000222214.4:n.636-35C=
ENST00000222214.9:c.636-35C= ENSP00000222214.4:n.636-35C=
ENST00000421816.6:n.614-35C=
ENST00000585420.5:n.1000+49C=
ENST00000590530.5:c.*76-35C= ENSP00000468452.1:n.*76-35C=
ENST00000591043.1:n.672-35C=
ENST00000591470.5:c.636-35C= ENSP00000466845.1:n.636-35C=
NM_000159.3:c.636-35C= NP_000150.1:n.636-35C=
NM_013976.3:c.636-35C= NP_039663.1:n.636-35C=
NR_102316.1:n.799-35C=
NR_102317.1:n.1051+49C=
XM_006722721.2:c.636-35C= XP_006722784.1:n.636-35C=
XM_011527899.1:c.636-35C= XP_011526201.1:n.636-35C=
XM_011527900.1:c.636-35C= XP_011526202.1:n.636-35C=
XM_011527899.2:c.636-35C= XP_011526201.1:n.636-35C=
XM_011527900.2:c.636-35C= XP_011526202.1:n.636-35C=
XM_017026580.1:c.636-35C= XP_016882069.1:n.636-35C=
NM_000159.4:c.636-35C= MANE Select NP_000150.1:n.636-35C=
NM_013976.4:c.636-35C= NP_039663.1:n.636-35C=
NM_013976.5:c.636-35C= NP_039663.1:n.636-35C=