Canonical Allele Identifier: CA2323624113
Gene: GCDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12897832C= , CM000681.2:g.12897832C= GRCh38
NC_000019.9:g.13008646C= , CM000681.1:g.13008646C= GRCh37
NC_000019.8:g.12869646C= NCBI36
NG_009292.1:g.11673C=
NG_033049.1:g.26441G=

Transcript Alleles

HGVS Amino-acid change
ENST00000222214.10:c.1212C= MANE Select ENSP00000222214.4:p.Ala404=
ENST00000222214.9:c.1212C= ENSP00000222214.4:p.Ala404=
ENST00000585420.5:n.1542C=
ENST00000590472.5:c.256C=
ENST00000590530.5:c.*652C= ENSP00000468452.1:n.*652C=
ENST00000591043.1:n.1522C=
ENST00000591050.1:c.179C=
ENST00000591470.5:c.1212C= ENSP00000466845.1:p.Ala404=
NM_000159.3:c.1212C= NP_000150.1:p.Ala404=
NM_013976.3:c.1212C= NP_039663.1:p.Ala404=
NR_102316.1:n.1375C=
NR_102317.1:n.1593C=
XM_006722721.2:c.1212C= XP_006722784.1:p.Ala404=
XM_011527899.1:c.1212C= XP_011526201.1:p.Ala404=
XM_011527900.1:c.1212C= XP_011526202.1:p.Ala404=
XM_011527899.2:c.1212C= XP_011526201.1:p.Ala404=
XM_011527900.2:c.1212C= XP_011526202.1:p.Ala404=
XM_017026580.1:c.1212C= XP_016882069.1:p.Ala404=
NM_000159.4:c.1212C= MANE Select NP_000150.1:p.Ala404=
NM_013976.4:c.1212C= NP_039663.1:p.Ala404=
NM_013976.5:c.1212C= NP_039663.1:p.Ala404=