Canonical Allele Identifier: CA437418543
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190126125T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408336T>C , CM000665.2:g.190408336T>C GRCh38
NC_000003.11:g.190126125T>C , CM000665.1:g.190126125T>C GRCh37
NC_000003.10:g.191608819T>C NCBI36
NG_008149.1:g.25285T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.405T>C MANE Select ENSP00000264734.3:p.Ser135=
ENST00000456423.2:c.115-1567T>C ENSP00000414136.2:n.115-1567T>C
ENST00000264734.2:c.615T>C ENSP00000264734.2:p.Ser205=
ENST00000456423.1:c.325-1567T>C ENSP00000414136.1:n.325-1567T>C
NM_006580.3:c.615T>C NP_006571.1:p.Ser205=
NM_001378492.1:c.405T>C NP_001365421.1:p.Ser135=
NM_001378493.1:c.405T>C NP_001365422.1:p.Ser135=
NM_006580.4:c.405T>C MANE Select NP_006571.2:p.Ser135=