Canonical Allele Identifier: CA355762361
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190106032G>C (hg19) chr3:g.190388243G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388243G>C , CM000665.2:g.190388243G>C GRCh38
NC_000003.11:g.190106032G>C , CM000665.1:g.190106032G>C GRCh37
NC_000003.10:g.191588726G>C NCBI36
NG_008149.1:g.5192G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.-87G>C MANE Select ENSP00000264734.3:n.-87G>C
ENST00000456423.2:c.-87G>C ENSP00000414136.2:n.-87G>C
ENST00000264734.2:c.124G>C ENSP00000264734.2:p.Glu42Gln
ENST00000456423.1:c.124G>C ENSP00000414136.1:p.Glu42Gln
ENST00000468220.1:n.306+13640G>C
NM_006580.3:c.124G>C NP_006571.1:p.Glu42Gln
NM_001378492.1:c.-87G>C NP_001365421.1:n.-87G>C
NM_001378493.1:c.-87G>C NP_001365422.1:n.-87G>C
NM_006580.4:c.-87G>C MANE Select NP_006571.2:n.-87G>C
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