Canonical Allele Identifier: CA1428775379
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387947T= , CM000665.2:g.190387947T= GRCh38
NC_000003.11:g.190105736T= , CM000665.1:g.190105736T= GRCh37
NC_000003.10:g.191588430T= NCBI36
NG_008149.1:g.4896T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-173T= ENSP00000264734.2:n.-173T=
ENST00000468220.1:n.306+13344T=
NM_006580.3:c.-173T= NP_006571.1:n.-173T=
NM_001378492.1:c.-93-290T= NP_001365421.1:n.-93-290T=
NM_001378493.1:c.-93-290T= NP_001365422.1:n.-93-290T=