Canonical Allele Identifier: CA355767303
Gene: CLDN16 HGNC NCBI

Linked Data

dbSNP Id: rs1719163555

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408466G>A , CM000665.2:g.190408466G>A GRCh38
NC_000003.11:g.190126255G>A , CM000665.1:g.190126255G>A GRCh37
NC_000003.10:g.191608949G>A NCBI36
NG_008149.1:g.25415G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.535G>A MANE Select ENSP00000264734.3:p.Ala179Thr
ENST00000456423.2:c.115-1437G>A ENSP00000414136.2:n.115-1437G>A
ENST00000264734.2:c.745G>A ENSP00000264734.2:p.Ala249Thr
ENST00000456423.1:c.325-1437G>A ENSP00000414136.1:n.325-1437G>A
NM_006580.3:c.745G>A NP_006571.1:p.Ala249Thr
NM_001378492.1:c.535G>A NP_001365421.1:p.Ala179Thr
NM_001378493.1:c.535G>A NP_001365422.1:p.Ala179Thr
NM_006580.4:c.535G>A MANE Select NP_006571.2:p.Ala179Thr