Canonical Allele Identifier: CA437418524
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190126104T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408315T>A , CM000665.2:g.190408315T>A GRCh38
NC_000003.11:g.190126104T>A , CM000665.1:g.190126104T>A GRCh37
NC_000003.10:g.191608798T>A NCBI36
NG_008149.1:g.25264T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.384T>A MANE Select ENSP00000264734.3:p.Gly128=
ENST00000456423.2:c.115-1588T>A ENSP00000414136.2:n.115-1588T>A
ENST00000264734.2:c.594T>A ENSP00000264734.2:p.Gly198=
ENST00000456423.1:c.325-1588T>A ENSP00000414136.1:n.325-1588T>A
NM_006580.3:c.594T>A NP_006571.1:p.Gly198=
NM_001378492.1:c.384T>A NP_001365421.1:p.Gly128=
NM_001378493.1:c.384T>A NP_001365422.1:p.Gly128=
NM_006580.4:c.384T>A MANE Select NP_006571.2:p.Gly128=