Canonical Allele Identifier: CA2323623146
Gene: GCDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12895916C= , CM000681.2:g.12895916C= GRCh38
NC_000019.9:g.13006730C= , CM000681.1:g.13006730C= GRCh37
NC_000019.8:g.12867730C= NCBI36
NG_009292.1:g.9757C=

Transcript Alleles

HGVS Amino-acid change
ENST00000222214.10:c.506-76C= MANE Select ENSP00000222214.4:n.506-76C=
ENST00000222214.9:c.506-76C= ENSP00000222214.4:n.506-76C=
ENST00000421816.6:n.484-76C=
ENST00000585420.5:n.871-76C=
ENST00000588905.5:c.470-76C= ENSP00000465770.1:n.470-76C=
ENST00000589039.5:c.443-76C= ENSP00000465618.1:n.443-76C=
ENST00000590530.5:c.561-76C= ENSP00000468452.1:n.561-76C=
ENST00000591043.1:n.542-76C=
ENST00000591470.5:c.506-76C= ENSP00000466845.1:n.506-76C=
NM_000159.3:c.506-76C= NP_000150.1:n.506-76C=
NM_013976.3:c.506-76C= NP_039663.1:n.506-76C=
NR_102316.1:n.669-76C=
NR_102317.1:n.922-76C=
XM_006722721.2:c.506-76C= XP_006722784.1:n.506-76C=
XM_011527899.1:c.506-76C= XP_011526201.1:n.506-76C=
XM_011527900.1:c.506-76C= XP_011526202.1:n.506-76C=
XM_011527899.2:c.506-76C= XP_011526201.1:n.506-76C=
XM_011527900.2:c.506-76C= XP_011526202.1:n.506-76C=
XM_017026580.1:c.506-76C= XP_016882069.1:n.506-76C=
NM_000159.4:c.506-76C= MANE Select NP_000150.1:n.506-76C=
NM_013976.4:c.506-76C= NP_039663.1:n.506-76C=
NM_013976.5:c.506-76C= NP_039663.1:n.506-76C=