Canonical Allele Identifier: CA2669041546
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404713A>G , CM000665.2:g.190404713A>G GRCh38
NC_000003.11:g.190122502A>G , CM000665.1:g.190122502A>G GRCh37
NC_000003.10:g.191605196A>G NCBI36
NG_008149.1:g.21662A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.218-49A>G MANE Select ENSP00000264734.3:n.218-49A>G
ENST00000456423.2:c.115-5190A>G ENSP00000414136.2:n.115-5190A>G
ENST00000264734.2:c.428-49A>G ENSP00000264734.2:n.428-49A>G
ENST00000456423.1:c.325-5190A>G ENSP00000414136.1:n.325-5190A>G
ENST00000468220.1:n.410-49A>G
NM_006580.3:c.428-49A>G NP_006571.1:n.428-49A>G
NM_001378492.1:c.218-49A>G NP_001365421.1:n.218-49A>G
NM_001378493.1:c.218-49A>G NP_001365422.1:n.218-49A>G
NM_006580.4:c.218-49A>G MANE Select NP_006571.2:n.218-49A>G