Canonical Allele Identifier: CA1428775465
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388040A= , CM000665.2:g.190388040A= GRCh38
NC_000003.11:g.190105829A= , CM000665.1:g.190105829A= GRCh37
NC_000003.10:g.191588523A= NCBI36
NG_008149.1:g.4989A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.2:c.-80A= ENSP00000264734.2:n.-80A=
ENST00000468220.1:n.306+13437A=
NM_006580.3:c.-80A= NP_006571.1:n.-80A=
NM_001378492.1:c.-93-197A= NP_001365421.1:n.-93-197A=
NM_001378493.1:c.-93-197A= NP_001365422.1:n.-93-197A=