Canonical Allele Identifier: CA355765483
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs146727044

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402361T>G , CM000665.2:g.190402361T>G GRCh38
NC_000003.11:g.190120150T>G , CM000665.1:g.190120150T>G GRCh37
NC_000003.10:g.191602844T>G NCBI36
NG_008149.1:g.19310T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.139T>G MANE Select ENSP00000264734.3:p.Trp47Gly
ENST00000456423.2:c.115-7542T>G ENSP00000414136.2:n.115-7542T>G
ENST00000264734.2:c.349T>G ENSP00000264734.2:p.Trp117Gly
ENST00000456423.1:c.325-7542T>G ENSP00000414136.1:n.325-7542T>G
ENST00000468220.1:n.331T>G
NM_006580.3:c.349T>G NP_006571.1:p.Trp117Gly
NM_001378492.1:c.139T>G NP_001365421.1:p.Trp47Gly
NM_001378493.1:c.139T>G NP_001365422.1:p.Trp47Gly
NM_006580.4:c.139T>G MANE Select NP_006571.2:p.Trp47Gly