Canonical Allele Identifier: CA1428762532
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408186C= , CM000665.2:g.190408186C= GRCh38
NC_000003.11:g.190125975C= , CM000665.1:g.190125975C= GRCh37
NC_000003.10:g.191608669C= NCBI36
NG_008149.1:g.25135C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.383-128C= MANE Select ENSP00000264734.3:n.383-128C=
ENST00000456423.2:c.115-1717C= ENSP00000414136.2:n.115-1717C=
ENST00000264734.2:c.593-128C= ENSP00000264734.2:n.593-128C=
ENST00000456423.1:c.325-1717C= ENSP00000414136.1:n.325-1717C=
NM_006580.3:c.593-128C= NP_006571.1:n.593-128C=
NM_001378492.1:c.383-128C= NP_001365421.1:n.383-128C=
NM_001378493.1:c.383-128C= NP_001365422.1:n.383-128C=
NM_006580.4:c.383-128C= MANE Select NP_006571.2:n.383-128C=