Canonical Allele Identifier: CA1428775392
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190387960T= , CM000665.2:g.190387960T= GRCh38
NC_000003.11:g.190105749T= , CM000665.1:g.190105749T= GRCh37
NC_000003.10:g.191588443T= NCBI36
NG_008149.1:g.4909T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-160T= ENSP00000264734.2:n.-160T=
ENST00000468220.1:n.306+13357T=
NM_006580.3:c.-160T= NP_006571.1:n.-160T=
NM_001378492.1:c.-93-277T= NP_001365421.1:n.-93-277T=
NM_001378493.1:c.-93-277T= NP_001365422.1:n.-93-277T=