Canonical Allele Identifier: CA2323622003
Gene: GCDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12893493T= , CM000681.2:g.12893493T= GRCh38
NC_000019.9:g.13004307T= , CM000681.1:g.13004307T= GRCh37
NC_000019.8:g.12865307T= NCBI36
NG_009292.1:g.7334T=

Transcript Alleles

HGVS Amino-acid change
ENST00000222214.10:c.345T= MANE Select ENSP00000222214.4:p.Cys115=
ENST00000222214.9:c.345T= ENSP00000222214.4:p.Cys115=
ENST00000421816.6:n.323T=
ENST00000585420.5:n.710T=
ENST00000587072.1:c.393T= ENSP00000468584.1:p.Cys131=
ENST00000587832.5:n.402T=
ENST00000588905.5:c.309T= ENSP00000465770.1:p.Cys103=
ENST00000589039.5:c.282T= ENSP00000465618.1:p.Cys94=
ENST00000590530.5:c.400T= ENSP00000468452.1:p.Cys134=
ENST00000590627.5:n.710T=
ENST00000591043.1:n.381T=
ENST00000591470.5:c.345T= ENSP00000466845.1:p.Cys115=
NM_000159.3:c.345T= NP_000150.1:p.Cys115=
NM_013976.3:c.345T= NP_039663.1:p.Cys115=
NR_102316.1:n.508T=
NR_102317.1:n.761T=
XM_006722721.2:c.345T= XP_006722784.1:p.Cys115=
XM_011527899.1:c.345T= XP_011526201.1:p.Cys115=
XM_011527900.1:c.345T= XP_011526202.1:p.Cys115=
XM_011527899.2:c.345T= XP_011526201.1:p.Cys115=
XM_011527900.2:c.345T= XP_011526202.1:p.Cys115=
XM_017026580.1:c.345T= XP_016882069.1:p.Cys115=
NM_000159.4:c.345T= MANE Select NP_000150.1:p.Cys115=
NM_013976.4:c.345T= NP_039663.1:p.Cys115=
NM_013976.5:c.345T= NP_039663.1:p.Cys115=