Canonical Allele Identifier: CA355767178
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408436G>C , CM000665.2:g.190408436G>C GRCh38
NC_000003.11:g.190126225G>C , CM000665.1:g.190126225G>C GRCh37
NC_000003.10:g.191608919G>C NCBI36
NG_008149.1:g.25385G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.505G>C MANE Select ENSP00000264734.3:p.Gly169Arg
ENST00000456423.2:c.115-1467G>C ENSP00000414136.2:n.115-1467G>C
ENST00000264734.2:c.715G>C ENSP00000264734.2:p.Gly239Arg
ENST00000456423.1:c.325-1467G>C ENSP00000414136.1:n.325-1467G>C
NM_006580.3:c.715G>C NP_006571.1:p.Gly239Arg
NM_001378492.1:c.505G>C NP_001365421.1:p.Gly169Arg
NM_001378493.1:c.505G>C NP_001365422.1:p.Gly169Arg
NM_006580.4:c.505G>C MANE Select NP_006571.2:p.Gly169Arg