Canonical Allele Identifier: CA2669054051
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387987_190387998del , CM000665.2:g.190387987_190387998del GRCh38
NC_000003.11:g.190105776_190105787del , CM000665.1:g.190105776_190105787del GRCh37
NC_000003.10:g.191588470_191588481del NCBI36
NG_008149.1:g.4936_4947del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-133_-122del ENSP00000264734.2:n.-133_-122del
ENST00000468220.1:n.306+13384_306+13395del
NM_006580.3:c.-133_-122del NP_006571.1:n.-133_-122del
NM_001378492.1:c.-93-250_-93-239del NP_001365421.1:n.-93-250_-93-239del
NM_001378493.1:c.-93-250_-93-239del NP_001365422.1:n.-93-250_-93-239del