Canonical Allele Identifier: CA1428757241

Gene: CLDN16

Linked Data

• dbSNP Id: rs1718991471
• gnomAD v4: 3-190402555-TTGTAATGGTTAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402556_190402567del , CM000665.2:g.190402556_190402567del	GRCh38
NC_000003.11:g.190120345_190120356del , CM000665.1:g.190120345_190120356del	GRCh37
NC_000003.10:g.191603039_191603050del	NCBI36
NG_008149.1:g.19505_19516del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.217+117_217+128del MANE Select	ENSP00000264734.3:n.217+117_217+128del
ENST00000456423.2:c.115-7347_115-7336del	ENSP00000414136.2:n.115-7347_115-7336del
ENST00000264734.2:c.427+117_427+128del	ENSP00000264734.2:n.427+117_427+128del
ENST00000456423.1:c.325-7347_325-7336del	ENSP00000414136.1:n.325-7347_325-7336del
ENST00000468220.1:n.409+117_409+128del
NM_006580.3:c.427+117_427+128del	NP_006571.1:n.427+117_427+128del
NM_001378492.1:c.217+117_217+128del	NP_001365421.1:n.217+117_217+128del
NM_001378493.1:c.217+117_217+128del	NP_001365422.1:n.217+117_217+128del
NM_006580.4:c.217+117_217+128del MANE Select	NP_006571.2:n.217+117_217+128del