Canonical Allele Identifier: CA2669041711
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408250G>T , CM000665.2:g.190408250G>T GRCh38
NC_000003.11:g.190126039G>T , CM000665.1:g.190126039G>T GRCh37
NC_000003.10:g.191608733G>T NCBI36
NG_008149.1:g.25199G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.383-64G>T MANE Select ENSP00000264734.3:n.383-64G>T
ENST00000456423.2:c.115-1653G>T ENSP00000414136.2:n.115-1653G>T
ENST00000264734.2:c.593-64G>T ENSP00000264734.2:n.593-64G>T
ENST00000456423.1:c.325-1653G>T ENSP00000414136.1:n.325-1653G>T
NM_006580.3:c.593-64G>T NP_006571.1:n.593-64G>T
NM_001378492.1:c.383-64G>T NP_001365421.1:n.383-64G>T
NM_001378493.1:c.383-64G>T NP_001365422.1:n.383-64G>T
NM_006580.4:c.383-64G>T MANE Select NP_006571.2:n.383-64G>T