Canonical Allele Identifier: CA437637190
Gene: CLDN16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.190106040G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190388251G>A , CM000665.2:g.190388251G>A GRCh38
NC_000003.11:g.190106040G>A , CM000665.1:g.190106040G>A GRCh37
NC_000003.10:g.191588734G>A NCBI36
NG_008149.1:g.5200G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.-79G>A MANE Select ENSP00000264734.3:n.-79G>A
ENST00000456423.2:c.-79G>A ENSP00000414136.2:n.-79G>A
ENST00000264734.2:c.132G>A ENSP00000264734.2:p.Gln44=
ENST00000456423.1:c.132G>A ENSP00000414136.1:p.Gln44=
ENST00000468220.1:n.306+13648G>A
NM_006580.3:c.132G>A NP_006571.1:p.Gln44=
NM_001378492.1:c.-79G>A NP_001365421.1:n.-79G>A
NM_001378493.1:c.-79G>A NP_001365422.1:n.-79G>A
NM_006580.4:c.-79G>A MANE Select NP_006571.2:n.-79G>A
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