Canonical Allele Identifier: CA437637073

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190105944_190105948del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388155_190388159del , CM000665.2:g.190388155_190388159del	GRCh38
NC_000003.11:g.190105944_190105948del , CM000665.1:g.190105944_190105948del	GRCh37
NC_000003.10:g.191588638_191588642del	NCBI36
NG_008149.1:g.5104_5108del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-175_-171del	ENSP00000414136.2:n.-175_-171del
ENST00000264734.2:c.36_40del	ENSP00000264734.2:p.Cys12Ter
ENST00000456423.1:c.36_40del	ENSP00000414136.1:p.Cys12Ter
ENST00000468220.1:n.306+13552_306+13556del
NM_006580.3:c.36_40del	NP_006571.1:p.Cys12Ter
NM_001378492.1:c.-93-82_-93-78del	NP_001365421.1:n.-93-82_-93-78del
NM_001378493.1:c.-93-82_-93-78del	NP_001365422.1:n.-93-82_-93-78del