Canonical Allele Identifier: CA1428759729
Gene: CLDN16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190405049A= , CM000665.2:g.190405049A= GRCh38
NC_000003.11:g.190122838A= , CM000665.1:g.190122838A= GRCh37
NC_000003.10:g.191605532A= NCBI36
NG_008149.1:g.21998A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.382+123A= MANE Select ENSP00000264734.3:n.382+123A=
ENST00000456423.2:c.115-4854A= ENSP00000414136.2:n.115-4854A=
ENST00000264734.2:c.592+123A= ENSP00000264734.2:n.592+123A=
ENST00000456423.1:c.325-4854A= ENSP00000414136.1:n.325-4854A=
NM_006580.3:c.592+123A= NP_006571.1:n.592+123A=
NM_001378492.1:c.382+123A= NP_001365421.1:n.382+123A=
NM_001378493.1:c.382+123A= NP_001365422.1:n.382+123A=
NM_006580.4:c.382+123A= MANE Select NP_006571.2:n.382+123A=
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