Canonical Allele Identifier: CA355762585

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190106141T>A (hg19) ; chr3:g.190388352T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388352T>A , CM000665.2:g.190388352T>A	GRCh38
NC_000003.11:g.190106141T>A , CM000665.1:g.190106141T>A	GRCh37
NC_000003.10:g.191588835T>A	NCBI36
NG_008149.1:g.5301T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264734.3:c.23T>A MANE Select	ENSP00000264734.3:p.Ile8Asn
ENST00000456423.2:c.23T>A	ENSP00000414136.2:p.Ile8Asn
ENST00000264734.2:c.233T>A	ENSP00000264734.2:p.Ile78Asn
ENST00000456423.1:c.233T>A	ENSP00000414136.1:p.Ile78Asn
ENST00000468220.1:n.306+13749T>A
NM_006580.3:c.233T>A	NP_006571.1:p.Ile78Asn
NM_001378492.1:c.23T>A	NP_001365421.1:p.Ile8Asn
NM_001378493.1:c.23T>A	NP_001365422.1:p.Ile8Asn
NM_006580.4:c.23T>A MANE Select	NP_006571.2:p.Ile8Asn