Canonical Allele Identifier: CA355767161
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408428G>T , CM000665.2:g.190408428G>T GRCh38
NC_000003.11:g.190126217G>T , CM000665.1:g.190126217G>T GRCh37
NC_000003.10:g.191608911G>T NCBI36
NG_008149.1:g.25377G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.497G>T MANE Select ENSP00000264734.3:p.Cys166Phe
ENST00000456423.2:c.115-1475G>T ENSP00000414136.2:n.115-1475G>T
ENST00000264734.2:c.707G>T ENSP00000264734.2:p.Cys236Phe
ENST00000456423.1:c.325-1475G>T ENSP00000414136.1:n.325-1475G>T
NM_006580.3:c.707G>T NP_006571.1:p.Cys236Phe
NM_001378492.1:c.497G>T NP_001365421.1:p.Cys166Phe
NM_001378493.1:c.497G>T NP_001365422.1:p.Cys166Phe
NM_006580.4:c.497G>T MANE Select NP_006571.2:p.Cys166Phe