Canonical Allele Identifier: CA1428762637
Gene: CLDN16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408316_190408317delinsAC , CM000665.2:g.190408316_190408317delinsAC GRCh38
NC_000003.11:g.190126105_190126106delinsAC , CM000665.1:g.190126105_190126106delinsAC GRCh37
NC_000003.10:g.191608799_191608800delinsAC NCBI36
NG_008149.1:g.25265_25266delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.385_386delinsAC MANE Select ENSP00000264734.3:p.Thr129=
ENST00000456423.2:c.115-1587_115-1586delinsAC ENSP00000414136.2:n.115-1587_115-1586delinsAC
ENST00000264734.2:c.595_596delinsAC ENSP00000264734.2:p.Thr199=
ENST00000456423.1:c.325-1587_325-1586delinsAC ENSP00000414136.1:n.325-1587_325-1586delinsAC
NM_006580.3:c.595_596delinsAC NP_006571.1:p.Thr199=
NM_001378492.1:c.385_386delinsAC NP_001365421.1:p.Thr129=
NM_001378493.1:c.385_386delinsAC NP_001365422.1:p.Thr129=
NM_006580.4:c.385_386delinsAC MANE Select NP_006571.2:p.Thr129=
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