Canonical Allele Identifier: CA904278975

Gene: CLDN16

Linked Data

• dbSNP Id: rs1220410147
• MyVariant Identifiers: chr3:g.190105757_190105758insC (hg19) ; chr3:g.190387968_190387969insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190387973dup , CM000665.2:g.190387973dup	GRCh38
NC_000003.11:g.190105762dup , CM000665.1:g.190105762dup	GRCh37
NC_000003.10:g.191588456dup	NCBI36
NG_008149.1:g.4922dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.2:c.-147dup	ENSP00000264734.2:n.-147dup
ENST00000468220.1:n.306+13370dup
NM_006580.3:c.-147dup	NP_006571.1:n.-147dup
NM_001378492.1:c.-93-264dup	NP_001365421.1:n.-93-264dup
NM_001378493.1:c.-93-264dup	NP_001365422.1:n.-93-264dup