Canonical Allele Identifier: CA1428759318
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404786T= , CM000665.2:g.190404786T= GRCh38
NC_000003.11:g.190122575T= , CM000665.1:g.190122575T= GRCh37
NC_000003.10:g.191605269T= NCBI36
NG_008149.1:g.21735T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.242T= MANE Select ENSP00000264734.3:p.Leu81=
ENST00000456423.2:c.115-5117T= ENSP00000414136.2:n.115-5117T=
ENST00000264734.2:c.452T= ENSP00000264734.2:p.Leu151=
ENST00000456423.1:c.325-5117T= ENSP00000414136.1:n.325-5117T=
ENST00000468220.1:n.434T=
NM_006580.3:c.452T= NP_006571.1:p.Leu151=
NM_001378492.1:c.242T= NP_001365421.1:p.Leu81=
NM_001378493.1:c.242T= NP_001365422.1:p.Leu81=
NM_006580.4:c.242T= MANE Select NP_006571.2:p.Leu81=