Canonical Allele Identifier: CA1057666487

Gene: CLDN16

Linked Data

• dbSNP Id: rs1718978129
• gnomAD v3: 3-190402129-A-T
• gnomAD v4: 3-190402129-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402129A>T , CM000665.2:g.190402129A>T	GRCh38
NC_000003.11:g.190119918A>T , CM000665.1:g.190119918A>T	GRCh37
NC_000003.10:g.191602612A>T	NCBI36
NG_008149.1:g.19078A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-208A>T MANE Select	ENSP00000264734.3:n.115-208A>T
ENST00000456423.2:c.115-7774A>T	ENSP00000414136.2:n.115-7774A>T
ENST00000264734.2:c.325-208A>T	ENSP00000264734.2:n.325-208A>T
ENST00000456423.1:c.325-7774A>T	ENSP00000414136.1:n.325-7774A>T
ENST00000468220.1:n.307-208A>T
NM_006580.3:c.325-208A>T	NP_006571.1:n.325-208A>T
NM_001378492.1:c.115-208A>T	NP_001365421.1:n.115-208A>T
NM_001378493.1:c.115-208A>T	NP_001365422.1:n.115-208A>T
NM_006580.4:c.115-208A>T MANE Select	NP_006571.2:n.115-208A>T