Canonical Allele Identifier: CA355766052

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190122599C>G (hg19) ; chr3:g.190404810C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404810C>G , CM000665.2:g.190404810C>G	GRCh38
NC_000003.11:g.190122599C>G , CM000665.1:g.190122599C>G	GRCh37
NC_000003.10:g.191605293C>G	NCBI36
NG_008149.1:g.21759C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.266C>G MANE Select	ENSP00000264734.3:p.Ala89Gly
ENST00000456423.2:c.115-5093C>G	ENSP00000414136.2:n.115-5093C>G
ENST00000264734.2:c.476C>G	ENSP00000264734.2:p.Ala159Gly
ENST00000456423.1:c.325-5093C>G	ENSP00000414136.1:n.325-5093C>G
ENST00000468220.1:n.458C>G
NM_006580.3:c.476C>G	NP_006571.1:p.Ala159Gly
NM_001378492.1:c.266C>G	NP_001365421.1:p.Ala89Gly
NM_001378493.1:c.266C>G	NP_001365422.1:p.Ala89Gly
NM_006580.4:c.266C>G MANE Select	NP_006571.2:p.Ala89Gly