Canonical Allele Identifier: CA1428775394
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387964T= , CM000665.2:g.190387964T= GRCh38
NC_000003.11:g.190105753T= , CM000665.1:g.190105753T= GRCh37
NC_000003.10:g.191588447T= NCBI36
NG_008149.1:g.4913T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-156T= ENSP00000264734.2:n.-156T=
ENST00000468220.1:n.306+13361T=
NM_006580.3:c.-156T= NP_006571.1:n.-156T=
NM_001378492.1:c.-93-273T= NP_001365421.1:n.-93-273T=
NM_001378493.1:c.-93-273T= NP_001365422.1:n.-93-273T=