Canonical Allele Identifier: CA1428762794
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408419G= , CM000665.2:g.190408419G= GRCh38
NC_000003.11:g.190126208G= , CM000665.1:g.190126208G= GRCh37
NC_000003.10:g.191608902G= NCBI36
NG_008149.1:g.25368G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.488G= MANE Select ENSP00000264734.3:p.Gly163=
ENST00000456423.2:c.115-1484G= ENSP00000414136.2:n.115-1484G=
ENST00000264734.2:c.698G= ENSP00000264734.2:p.Gly233=
ENST00000456423.1:c.325-1484G= ENSP00000414136.1:n.325-1484G=
NM_006580.3:c.698G= NP_006571.1:p.Gly233=
NM_001378492.1:c.488G= NP_001365421.1:p.Gly163=
NM_001378493.1:c.488G= NP_001365422.1:p.Gly163=
NM_006580.4:c.488G= MANE Select NP_006571.2:p.Gly163=