Canonical Allele Identifier: CA1428759110

Gene: CLDN16

Linked Data

• dbSNP Id: rs1421414809
• gnomAD v4: 3-190404620-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404620T>G , CM000665.2:g.190404620T>G	GRCh38
NC_000003.11:g.190122409T>G , CM000665.1:g.190122409T>G	GRCh37
NC_000003.10:g.191605103T>G	NCBI36
NG_008149.1:g.21569T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-142T>G MANE Select	ENSP00000264734.3:n.218-142T>G
ENST00000456423.2:c.115-5283T>G	ENSP00000414136.2:n.115-5283T>G
ENST00000264734.2:c.428-142T>G	ENSP00000264734.2:n.428-142T>G
ENST00000456423.1:c.325-5283T>G	ENSP00000414136.1:n.325-5283T>G
ENST00000468220.1:n.410-142T>G
NM_006580.3:c.428-142T>G	NP_006571.1:n.428-142T>G
NM_001378492.1:c.218-142T>G	NP_001365421.1:n.218-142T>G
NM_001378493.1:c.218-142T>G	NP_001365422.1:n.218-142T>G
NM_006580.4:c.218-142T>G MANE Select	NP_006571.2:n.218-142T>G