Canonical Allele Identifier: CA1428756630
Gene: CLDN16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402089G= , CM000665.2:g.190402089G= GRCh38
NC_000003.11:g.190119878G= , CM000665.1:g.190119878G= GRCh37
NC_000003.10:g.191602572G= NCBI36
NG_008149.1:g.19038G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.115-248G= MANE Select ENSP00000264734.3:n.115-248G=
ENST00000456423.2:c.115-7814G= ENSP00000414136.2:n.115-7814G=
ENST00000264734.2:c.325-248G= ENSP00000264734.2:n.325-248G=
ENST00000456423.1:c.325-7814G= ENSP00000414136.1:n.325-7814G=
ENST00000468220.1:n.307-248G=
NM_006580.3:c.325-248G= NP_006571.1:n.325-248G=
NM_001378492.1:c.115-248G= NP_001365421.1:n.115-248G=
NM_001378493.1:c.115-248G= NP_001365422.1:n.115-248G=
NM_006580.4:c.115-248G= MANE Select NP_006571.2:n.115-248G=
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