Canonical Allele Identifier: CA1428759175

Gene: CLDN16

Linked Data

• dbSNP Id: rs1371004451
• gnomAD v4: 3-190404692-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404692G>A , CM000665.2:g.190404692G>A	GRCh38
NC_000003.11:g.190122481G>A , CM000665.1:g.190122481G>A	GRCh37
NC_000003.10:g.191605175G>A	NCBI36
NG_008149.1:g.21641G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-70G>A MANE Select	ENSP00000264734.3:n.218-70G>A
ENST00000456423.2:c.115-5211G>A	ENSP00000414136.2:n.115-5211G>A
ENST00000264734.2:c.428-70G>A	ENSP00000264734.2:n.428-70G>A
ENST00000456423.1:c.325-5211G>A	ENSP00000414136.1:n.325-5211G>A
ENST00000468220.1:n.410-70G>A
NM_006580.3:c.428-70G>A	NP_006571.1:n.428-70G>A
NM_001378492.1:c.218-70G>A	NP_001365421.1:n.218-70G>A
NM_001378493.1:c.218-70G>A	NP_001365422.1:n.218-70G>A
NM_006580.4:c.218-70G>A MANE Select	NP_006571.2:n.218-70G>A