Canonical Allele Identifier: CA2323621111
Gene: GCDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12891819T= , CM000681.2:g.12891819T= GRCh38
NC_000019.9:g.13002633T= , CM000681.1:g.13002633T= GRCh37
NC_000019.8:g.12863633T= NCBI36
NG_009292.1:g.5660T=
NG_013087.1:g.385A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222214.10:c.128-12T= MANE Select ENSP00000222214.4:n.128-12T=
ENST00000222214.9:c.128-12T= ENSP00000222214.4:n.128-12T=
ENST00000421816.6:n.169-12T=
ENST00000585420.5:n.481T=
ENST00000585760.5:n.164-12T=
ENST00000587072.1:c.128-12T= ENSP00000468584.1:n.128-12T=
ENST00000587832.5:n.185-12T=
ENST00000588905.5:c.92-12T= ENSP00000465770.1:n.92-12T=
ENST00000589039.5:c.128-12T= ENSP00000465618.1:n.128-12T=
ENST00000590445.5:c.*5-12T= ENSP00000468125.1:n.*5-12T=
ENST00000590530.5:c.128-12T= ENSP00000468452.1:n.128-12T=
ENST00000590627.5:n.481T=
ENST00000591043.1:n.164-12T=
ENST00000591470.5:c.128-12T= ENSP00000466845.1:n.128-12T=
NM_000159.3:c.128-12T= NP_000150.1:n.128-12T=
NM_013976.3:c.128-12T= NP_039663.1:n.128-12T=
NR_102316.1:n.236-12T=
NR_102317.1:n.532T=
XM_006722721.2:c.128-12T= XP_006722784.1:n.128-12T=
XM_011527899.1:c.128-12T= XP_011526201.1:n.128-12T=
XM_011527900.1:c.128-12T= XP_011526202.1:n.128-12T=
XM_011527899.2:c.128-12T= XP_011526201.1:n.128-12T=
XM_011527900.2:c.128-12T= XP_011526202.1:n.128-12T=
XM_017026580.1:c.128-12T= XP_016882069.1:n.128-12T=
NM_000159.4:c.128-12T= MANE Select NP_000150.1:n.128-12T=
NM_013976.4:c.128-12T= NP_039663.1:n.128-12T=
NM_013976.5:c.128-12T= NP_039663.1:n.128-12T=