Canonical Allele Identifier: CA355766943
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408329T>G , CM000665.2:g.190408329T>G GRCh38
NC_000003.11:g.190126118T>G , CM000665.1:g.190126118T>G GRCh37
NC_000003.10:g.191608812T>G NCBI36
NG_008149.1:g.25278T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.398T>G MANE Select ENSP00000264734.3:p.Ile133Ser
ENST00000456423.2:c.115-1574T>G ENSP00000414136.2:n.115-1574T>G
ENST00000264734.2:c.608T>G ENSP00000264734.2:p.Ile203Ser
ENST00000456423.1:c.325-1574T>G ENSP00000414136.1:n.325-1574T>G
NM_006580.3:c.608T>G NP_006571.1:p.Ile203Ser
NM_001378492.1:c.398T>G NP_001365421.1:p.Ile133Ser
NM_001378493.1:c.398T>G NP_001365422.1:p.Ile133Ser
NM_006580.4:c.398T>G MANE Select NP_006571.2:p.Ile133Ser