Canonical Allele Identifier: CA1428759442
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404840G= , CM000665.2:g.190404840G= GRCh38
NC_000003.11:g.190122629G= , CM000665.1:g.190122629G= GRCh37
NC_000003.10:g.191605323G= NCBI36
NG_008149.1:g.21789G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.296G= MANE Select ENSP00000264734.3:p.Gly99=
ENST00000456423.2:c.115-5063G= ENSP00000414136.2:n.115-5063G=
ENST00000264734.2:c.506G= ENSP00000264734.2:p.Gly169=
ENST00000456423.1:c.325-5063G= ENSP00000414136.1:n.325-5063G=
ENST00000468220.1:n.488G=
NM_006580.3:c.506G= NP_006571.1:p.Gly169=
NM_001378492.1:c.296G= NP_001365421.1:p.Gly99=
NM_001378493.1:c.296G= NP_001365422.1:p.Gly99=
NM_006580.4:c.296G= MANE Select NP_006571.2:p.Gly99=