Canonical Allele Identifier: CA1428759750
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190405079C= , CM000665.2:g.190405079C= GRCh38
NC_000003.11:g.190122868C= , CM000665.1:g.190122868C= GRCh37
NC_000003.10:g.191605562C= NCBI36
NG_008149.1:g.22028C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.382+153C= MANE Select ENSP00000264734.3:n.382+153C=
ENST00000456423.2:c.115-4824C= ENSP00000414136.2:n.115-4824C=
ENST00000264734.2:c.592+153C= ENSP00000264734.2:n.592+153C=
ENST00000456423.1:c.325-4824C= ENSP00000414136.1:n.325-4824C=
NM_006580.3:c.592+153C= NP_006571.1:n.592+153C=
NM_001378492.1:c.382+153C= NP_001365421.1:n.382+153C=
NM_001378493.1:c.382+153C= NP_001365422.1:n.382+153C=
NM_006580.4:c.382+153C= MANE Select NP_006571.2:n.382+153C=