Canonical Allele Identifier: CA2669041460
Gene: CLDN16 HGNC NCBI

Linked Data

gnomAD v4: 3-190404639-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404639T>A , CM000665.2:g.190404639T>A GRCh38
NC_000003.11:g.190122428T>A , CM000665.1:g.190122428T>A GRCh37
NC_000003.10:g.191605122T>A NCBI36
NG_008149.1:g.21588T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.218-123T>A MANE Select ENSP00000264734.3:n.218-123T>A
ENST00000456423.2:c.115-5264T>A ENSP00000414136.2:n.115-5264T>A
ENST00000264734.2:c.428-123T>A ENSP00000264734.2:n.428-123T>A
ENST00000456423.1:c.325-5264T>A ENSP00000414136.1:n.325-5264T>A
ENST00000468220.1:n.410-123T>A
NM_006580.3:c.428-123T>A NP_006571.1:n.428-123T>A
NM_001378492.1:c.218-123T>A NP_001365421.1:n.218-123T>A
NM_001378493.1:c.218-123T>A NP_001365422.1:n.218-123T>A
NM_006580.4:c.218-123T>A MANE Select NP_006571.2:n.218-123T>A
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