Canonical Allele Identifier: CA355765478
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190402359T>G , CM000665.2:g.190402359T>G GRCh38
NC_000003.11:g.190120148T>G , CM000665.1:g.190120148T>G GRCh37
NC_000003.10:g.191602842T>G NCBI36
NG_008149.1:g.19308T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.137T>G MANE Select ENSP00000264734.3:p.Leu46Arg
ENST00000456423.2:c.115-7544T>G ENSP00000414136.2:n.115-7544T>G
ENST00000264734.2:c.347T>G ENSP00000264734.2:p.Leu116Arg
ENST00000456423.1:c.325-7544T>G ENSP00000414136.1:n.325-7544T>G
ENST00000468220.1:n.329T>G
NM_006580.3:c.347T>G NP_006571.1:p.Leu116Arg
NM_001378492.1:c.137T>G NP_001365421.1:p.Leu46Arg
NM_001378493.1:c.137T>G NP_001365422.1:p.Leu46Arg
NM_006580.4:c.137T>G MANE Select NP_006571.2:p.Leu46Arg