Canonical Allele Identifier: CA437418499

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190122693T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404904T>G , CM000665.2:g.190404904T>G	GRCh38
NC_000003.11:g.190122693T>G , CM000665.1:g.190122693T>G	GRCh37
NC_000003.10:g.191605387T>G	NCBI36
NG_008149.1:g.21853T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.360T>G MANE Select	ENSP00000264734.3:p.Ala120=
ENST00000456423.2:c.115-4999T>G	ENSP00000414136.2:n.115-4999T>G
ENST00000264734.2:c.570T>G	ENSP00000264734.2:p.Ala190=
ENST00000456423.1:c.325-4999T>G	ENSP00000414136.1:n.325-4999T>G
ENST00000468220.1:n.552T>G
NM_006580.3:c.570T>G	NP_006571.1:p.Ala190=
NM_001378492.1:c.360T>G	NP_001365421.1:p.Ala120=
NM_001378493.1:c.360T>G	NP_001365422.1:p.Ala120=
NM_006580.4:c.360T>G MANE Select	NP_006571.2:p.Ala120=