Canonical Allele Identifier: CA355768489
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190127738T>A (hg19) chr3:g.190409949T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190409949T>A , CM000665.2:g.190409949T>A GRCh38
NC_000003.11:g.190127738T>A , CM000665.1:g.190127738T>A GRCh37
NC_000003.10:g.191610432T>A NCBI36
NG_008149.1:g.26898T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.621T>A MANE Select ENSP00000264734.3:p.Tyr207Ter
ENST00000456423.2:c.*11T>A ENSP00000414136.2:n.*11T>A
ENST00000264734.2:c.831T>A ENSP00000264734.2:p.Tyr277Ter
ENST00000456423.1:c.371T>A ENSP00000414136.1:n.371T>A
NM_006580.3:c.831T>A NP_006571.1:p.Tyr277Ter
NM_001378492.1:c.621T>A NP_001365421.1:p.Tyr207Ter
NM_001378493.1:c.621T>A NP_001365422.1:p.Tyr207Ter
NM_006580.4:c.621T>A MANE Select NP_006571.2:p.Tyr207Ter
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