Canonical Allele Identifier: CA904290960
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1455600312

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408135A>G , CM000665.2:g.190408135A>G GRCh38
NC_000003.11:g.190125924A>G , CM000665.1:g.190125924A>G GRCh37
NC_000003.10:g.191608618A>G NCBI36
NG_008149.1:g.25084A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.383-179A>G MANE Select ENSP00000264734.3:n.383-179A>G
ENST00000456423.2:c.115-1768A>G ENSP00000414136.2:n.115-1768A>G
ENST00000264734.2:c.593-179A>G ENSP00000264734.2:n.593-179A>G
ENST00000456423.1:c.325-1768A>G ENSP00000414136.1:n.325-1768A>G
NM_006580.3:c.593-179A>G NP_006571.1:n.593-179A>G
NM_001378492.1:c.383-179A>G NP_001365421.1:n.383-179A>G
NM_001378493.1:c.383-179A>G NP_001365422.1:n.383-179A>G
NM_006580.4:c.383-179A>G MANE Select NP_006571.2:n.383-179A>G