Canonical Allele Identifier: CA2753685

Gene: CLDN16

Linked Data

• dbSNP Id: rs777659077
• ExAC: 3:190105964 A / G
• gnomAD v2: 3-190105964-A-G
• gnomAD v4: 3-190388175-A-G
• MyVariant Identifiers: chr3:g.190105964A>G (hg19) ; chr3:g.190388175A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388175A>G , CM000665.2:g.190388175A>G	GRCh38
NC_000003.11:g.190105964A>G , CM000665.1:g.190105964A>G	GRCh37
NC_000003.10:g.191588658A>G	NCBI36
NG_008149.1:g.5124A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.-155A>G MANE Select	ENSP00000264734.3:n.-155A>G
ENST00000456423.2:c.-155A>G	ENSP00000414136.2:n.-155A>G
ENST00000264734.2:c.56A>G	ENSP00000264734.2:p.Asn19Ser
ENST00000456423.1:c.56A>G	ENSP00000414136.1:p.Asn19Ser
ENST00000468220.1:n.306+13572A>G
NM_006580.3:c.56A>G	NP_006571.1:p.Asn19Ser
NM_001378492.1:c.-93-62A>G	NP_001365421.1:n.-93-62A>G
NM_001378493.1:c.-93-62A>G	NP_001365422.1:n.-93-62A>G
NM_006580.4:c.-155A>G MANE Select	NP_006571.2:n.-155A>G