Canonical Allele Identifier: CA355765956

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190122551T>G (hg19) ; chr3:g.190404762T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404762T>G , CM000665.2:g.190404762T>G	GRCh38
NC_000003.11:g.190122551T>G , CM000665.1:g.190122551T>G	GRCh37
NC_000003.10:g.191605245T>G	NCBI36
NG_008149.1:g.21711T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264734.3:c.218T>G MANE Select	ENSP00000264734.3:p.Leu73Trp
ENST00000456423.2:c.115-5141T>G	ENSP00000414136.2:n.115-5141T>G
ENST00000264734.2:c.428T>G	ENSP00000264734.2:p.Leu143Trp
ENST00000456423.1:c.325-5141T>G	ENSP00000414136.1:n.325-5141T>G
ENST00000468220.1:n.410T>G
NM_006580.3:c.428T>G	NP_006571.1:p.Leu143Trp
NM_001378492.1:c.218T>G	NP_001365421.1:p.Leu73Trp
NM_001378493.1:c.218T>G	NP_001365422.1:p.Leu73Trp
NM_006580.4:c.218T>G MANE Select	NP_006571.2:p.Leu73Trp