Canonical Allele Identifier: CA1428775488
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388070C= , CM000665.2:g.190388070C= GRCh38
NC_000003.11:g.190105859C= , CM000665.1:g.190105859C= GRCh37
NC_000003.10:g.191588553C= NCBI36
NG_008149.1:g.5019C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-50C= ENSP00000264734.2:n.-50C=
ENST00000468220.1:n.306+13467C=
NM_006580.3:c.-50C= NP_006571.1:n.-50C=
NM_001378492.1:c.-93-167C= NP_001365421.1:n.-93-167C=
NM_001378493.1:c.-93-167C= NP_001365422.1:n.-93-167C=