Canonical Allele Identifier: CA1428775388
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387959C= , CM000665.2:g.190387959C= GRCh38
NC_000003.11:g.190105748C= , CM000665.1:g.190105748C= GRCh37
NC_000003.10:g.191588442C= NCBI36
NG_008149.1:g.4908C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-161C= ENSP00000264734.2:n.-161C=
ENST00000468220.1:n.306+13356C=
NM_006580.3:c.-161C= NP_006571.1:n.-161C=
NM_001378492.1:c.-93-278C= NP_001365421.1:n.-93-278C=
NM_001378493.1:c.-93-278C= NP_001365422.1:n.-93-278C=