Canonical Allele Identifier: CA355765440

Gene: CLDN16

Linked Data

• gnomAD v4: 3-190402350-G-A
• MyVariant Identifiers: chr3:g.190120139G>A (hg19) ; chr3:g.190402350G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402350G>A , CM000665.2:g.190402350G>A	GRCh38
NC_000003.11:g.190120139G>A , CM000665.1:g.190120139G>A	GRCh37
NC_000003.10:g.191602833G>A	NCBI36
NG_008149.1:g.19299G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.128G>A MANE Select	ENSP00000264734.3:p.Cys43Tyr
ENST00000456423.2:c.115-7553G>A	ENSP00000414136.2:n.115-7553G>A
ENST00000264734.2:c.338G>A	ENSP00000264734.2:p.Cys113Tyr
ENST00000456423.1:c.325-7553G>A	ENSP00000414136.1:n.325-7553G>A
ENST00000468220.1:n.320G>A
NM_006580.3:c.338G>A	NP_006571.1:p.Cys113Tyr
NM_001378492.1:c.128G>A	NP_001365421.1:p.Cys43Tyr
NM_001378493.1:c.128G>A	NP_001365422.1:p.Cys43Tyr
NM_006580.4:c.128G>A MANE Select	NP_006571.2:p.Cys43Tyr