Canonical Allele Identifier: CA2323624055
Gene: GCDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12897728C= , CM000681.2:g.12897728C= GRCh38
NC_000019.9:g.13008542C= , CM000681.1:g.13008542C= GRCh37
NC_000019.8:g.12869542C= NCBI36
NG_009292.1:g.11569C=
NG_033049.1:g.26545G=

Transcript Alleles

HGVS Amino-acid change
ENST00000222214.10:c.1108C= MANE Select ENSP00000222214.4:p.Leu370=
ENST00000222214.9:c.1108C= ENSP00000222214.4:p.Leu370=
ENST00000585420.5:n.1438C=
ENST00000590472.5:c.152C=
ENST00000590530.5:c.*548C= ENSP00000468452.1:n.*548C=
ENST00000591043.1:n.1418C=
ENST00000591050.1:c.75C=
ENST00000591470.5:c.1108C= ENSP00000466845.1:p.Leu370=
NM_000159.3:c.1108C= NP_000150.1:p.Leu370=
NM_013976.3:c.1108C= NP_039663.1:p.Leu370=
NR_102316.1:n.1271C=
NR_102317.1:n.1489C=
XM_006722721.2:c.1108C= XP_006722784.1:p.Leu370=
XM_011527899.1:c.1108C= XP_011526201.1:p.Leu370=
XM_011527900.1:c.1108C= XP_011526202.1:p.Leu370=
XM_011527899.2:c.1108C= XP_011526201.1:p.Leu370=
XM_011527900.2:c.1108C= XP_011526202.1:p.Leu370=
XM_017026580.1:c.1108C= XP_016882069.1:p.Leu370=
NM_000159.4:c.1108C= MANE Select NP_000150.1:p.Leu370=
NM_013976.4:c.1108C= NP_039663.1:p.Leu370=
NM_013976.5:c.1108C= NP_039663.1:p.Leu370=