Canonical Allele Identifier: CA1428762669
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408335C= , CM000665.2:g.190408335C= GRCh38
NC_000003.11:g.190126124C= , CM000665.1:g.190126124C= GRCh37
NC_000003.10:g.191608818C= NCBI36
NG_008149.1:g.25284C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.404C= MANE Select ENSP00000264734.3:p.Ser135=
ENST00000456423.2:c.115-1568C= ENSP00000414136.2:n.115-1568C=
ENST00000264734.2:c.614C= ENSP00000264734.2:p.Ser205=
ENST00000456423.1:c.325-1568C= ENSP00000414136.1:n.325-1568C=
NM_006580.3:c.614C= NP_006571.1:p.Ser205=
NM_001378492.1:c.404C= NP_001365421.1:p.Ser135=
NM_001378493.1:c.404C= NP_001365422.1:p.Ser135=
NM_006580.4:c.404C= MANE Select NP_006571.2:p.Ser135=