Canonical Allele Identifier: CA437418388

Gene: CLDN16

Linked Data

• MyVariant Identifiers: chr3:g.190120215T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402426T>A , CM000665.2:g.190402426T>A	GRCh38
NC_000003.11:g.190120215T>A , CM000665.1:g.190120215T>A	GRCh37
NC_000003.10:g.191602909T>A	NCBI36
NG_008149.1:g.19375T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.204T>A MANE Select	ENSP00000264734.3:p.Leu68=
ENST00000456423.2:c.115-7477T>A	ENSP00000414136.2:n.115-7477T>A
ENST00000264734.2:c.414T>A	ENSP00000264734.2:p.Leu138=
ENST00000456423.1:c.325-7477T>A	ENSP00000414136.1:n.325-7477T>A
ENST00000468220.1:n.396T>A
NM_006580.3:c.414T>A	NP_006571.1:p.Leu138=
NM_001378492.1:c.204T>A	NP_001365421.1:p.Leu68=
NM_001378493.1:c.204T>A	NP_001365422.1:p.Leu68=
NM_006580.4:c.204T>A MANE Select	NP_006571.2:p.Leu68=