Canonical Allele Identifier: CA904287072

Gene: CLDN16

Linked Data

• dbSNP Id: rs1383456250
• gnomAD v3: 3-190402071-G-A
• gnomAD v4: 3-190402071-G-A
• MyVariant Identifiers: chr3:g.190119860G>A (hg19) ; chr3:g.190402071G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402071G>A , CM000665.2:g.190402071G>A	GRCh38
NC_000003.11:g.190119860G>A , CM000665.1:g.190119860G>A	GRCh37
NC_000003.10:g.191602554G>A	NCBI36
NG_008149.1:g.19020G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-266G>A MANE Select	ENSP00000264734.3:n.115-266G>A
ENST00000456423.2:c.115-7832G>A	ENSP00000414136.2:n.115-7832G>A
ENST00000264734.2:c.325-266G>A	ENSP00000264734.2:n.325-266G>A
ENST00000456423.1:c.325-7832G>A	ENSP00000414136.1:n.325-7832G>A
ENST00000468220.1:n.307-266G>A
NM_006580.3:c.325-266G>A	NP_006571.1:n.325-266G>A
NM_001378492.1:c.115-266G>A	NP_001365421.1:n.115-266G>A
NM_001378493.1:c.115-266G>A	NP_001365422.1:n.115-266G>A
NM_006580.4:c.115-266G>A MANE Select	NP_006571.2:n.115-266G>A