Canonical Allele Identifier: CA1428757387
Gene: CLDN16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402692G= , CM000665.2:g.190402692G= GRCh38
NC_000003.11:g.190120481G= , CM000665.1:g.190120481G= GRCh37
NC_000003.10:g.191603175G= NCBI36
NG_008149.1:g.19641G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.217+253G= MANE Select ENSP00000264734.3:n.217+253G=
ENST00000456423.2:c.115-7211G= ENSP00000414136.2:n.115-7211G=
ENST00000264734.2:c.427+253G= ENSP00000264734.2:n.427+253G=
ENST00000456423.1:c.325-7211G= ENSP00000414136.1:n.325-7211G=
ENST00000468220.1:n.409+253G=
NM_006580.3:c.427+253G= NP_006571.1:n.427+253G=
NM_001378492.1:c.217+253G= NP_001365421.1:n.217+253G=
NM_001378493.1:c.217+253G= NP_001365422.1:n.217+253G=
NM_006580.4:c.217+253G= MANE Select NP_006571.2:n.217+253G=
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