Canonical Allele Identifier: CA2323623317
Gene: GCDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12896249G= , CM000681.2:g.12896249G= GRCh38
NC_000019.9:g.13007063G= , CM000681.1:g.13007063G= GRCh37
NC_000019.8:g.12868063G= NCBI36
NG_009292.1:g.10090G=

Transcript Alleles

HGVS Amino-acid change
ENST00000222214.10:c.680G= MANE Select ENSP00000222214.4:p.Arg227=
ENST00000222214.9:c.680G= ENSP00000222214.4:p.Arg227=
ENST00000421816.6:n.658G=
ENST00000585420.5:n.1010G=
ENST00000590530.5:c.*120G= ENSP00000468452.1:n.*120G=
ENST00000591043.1:n.716G=
ENST00000591470.5:c.680G= ENSP00000466845.1:p.Arg227=
NM_000159.3:c.680G= NP_000150.1:p.Arg227=
NM_013976.3:c.680G= NP_039663.1:p.Arg227=
NR_102316.1:n.843G=
NR_102317.1:n.1061G=
XM_006722721.2:c.680G= XP_006722784.1:p.Arg227=
XM_011527899.1:c.680G= XP_011526201.1:p.Arg227=
XM_011527900.1:c.680G= XP_011526202.1:p.Arg227=
XM_011527899.2:c.680G= XP_011526201.1:p.Arg227=
XM_011527900.2:c.680G= XP_011526202.1:p.Arg227=
XM_017026580.1:c.680G= XP_016882069.1:p.Arg227=
NM_000159.4:c.680G= MANE Select NP_000150.1:p.Arg227=
NM_013976.4:c.680G= NP_039663.1:p.Arg227=
NM_013976.5:c.680G= NP_039663.1:p.Arg227=