Canonical Allele Identifier: CA1428762577
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408248A= , CM000665.2:g.190408248A= GRCh38
NC_000003.11:g.190126037A= , CM000665.1:g.190126037A= GRCh37
NC_000003.10:g.191608731A= NCBI36
NG_008149.1:g.25197A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.383-66A= MANE Select ENSP00000264734.3:n.383-66A=
ENST00000456423.2:c.115-1655A= ENSP00000414136.2:n.115-1655A=
ENST00000264734.2:c.593-66A= ENSP00000264734.2:n.593-66A=
ENST00000456423.1:c.325-1655A= ENSP00000414136.1:n.325-1655A=
NM_006580.3:c.593-66A= NP_006571.1:n.593-66A=
NM_001378492.1:c.383-66A= NP_001365421.1:n.383-66A=
NM_001378493.1:c.383-66A= NP_001365422.1:n.383-66A=
NM_006580.4:c.383-66A= MANE Select NP_006571.2:n.383-66A=