Canonical Allele Identifier: CA904287149

Gene: CLDN16

Linked Data

• dbSNP Id: rs1411831296
• MyVariant Identifiers: chr3:g.190119945del (hg19) ; chr3:g.190402156del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402157del , CM000665.2:g.190402157del	GRCh38
NC_000003.11:g.190119946del , CM000665.1:g.190119946del	GRCh37
NC_000003.10:g.191602640del	NCBI36
NG_008149.1:g.19106del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-180del MANE Select	ENSP00000264734.3:n.115-180del
ENST00000456423.2:c.115-7746del	ENSP00000414136.2:n.115-7746del
ENST00000264734.2:c.325-180del	ENSP00000264734.2:n.325-180del
ENST00000456423.1:c.325-7746del	ENSP00000414136.1:n.325-7746del
ENST00000468220.1:n.307-180del
NM_006580.3:c.325-180del	NP_006571.1:n.325-180del
NM_001378492.1:c.115-180del	NP_001365421.1:n.115-180del
NM_001378493.1:c.115-180del	NP_001365422.1:n.115-180del
NM_006580.4:c.115-180del MANE Select	NP_006571.2:n.115-180del