Canonical Allele Identifier: CA437637320
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190106142C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388353C>A , CM000665.2:g.190388353C>A GRCh38
NC_000003.11:g.190106142C>A , CM000665.1:g.190106142C>A GRCh37
NC_000003.10:g.191588836C>A NCBI36
NG_008149.1:g.5302C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.24C>A MANE Select ENSP00000264734.3:p.Ile8=
ENST00000456423.2:c.24C>A ENSP00000414136.2:p.Ile8=
ENST00000264734.2:c.234C>A ENSP00000264734.2:p.Ile78=
ENST00000456423.1:c.234C>A ENSP00000414136.1:p.Ile78=
ENST00000468220.1:n.306+13750C>A
NM_006580.3:c.234C>A NP_006571.1:p.Ile78=
NM_001378492.1:c.24C>A NP_001365421.1:p.Ile8=
NM_001378493.1:c.24C>A NP_001365422.1:p.Ile8=
NM_006580.4:c.24C>A MANE Select NP_006571.2:p.Ile8=
Search 100 bp 5'
Search 100 bp 3'