Canonical Allele Identifier: CA355765964
Gene: CLDN16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190404765A>C , CM000665.2:g.190404765A>C GRCh38
NC_000003.11:g.190122554A>C , CM000665.1:g.190122554A>C GRCh37
NC_000003.10:g.191605248A>C NCBI36
NG_008149.1:g.21714A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264734.3:c.221A>C MANE Select ENSP00000264734.3:p.Lys74Thr
ENST00000456423.2:c.115-5138A>C ENSP00000414136.2:n.115-5138A>C
ENST00000264734.2:c.431A>C ENSP00000264734.2:p.Lys144Thr
ENST00000456423.1:c.325-5138A>C ENSP00000414136.1:n.325-5138A>C
ENST00000468220.1:n.413A>C
NM_006580.3:c.431A>C NP_006571.1:p.Lys144Thr
NM_001378492.1:c.221A>C NP_001365421.1:p.Lys74Thr
NM_001378493.1:c.221A>C NP_001365422.1:p.Lys74Thr
NM_006580.4:c.221A>C MANE Select NP_006571.2:p.Lys74Thr