Canonical Allele Identifier: CA1428775593

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388141T= , CM000665.2:g.190388141T=	GRCh38
NC_000003.11:g.190105930T= , CM000665.1:g.190105930T=	GRCh37
NC_000003.10:g.191588624T=	NCBI36
NG_008149.1:g.5090T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-189T=	ENSP00000414136.2:n.-189T=
ENST00000264734.2:c.22T=	ENSP00000264734.2:p.Leu8=
ENST00000456423.1:c.22T=	ENSP00000414136.1:p.Leu8=
ENST00000468220.1:n.306+13538T=
NM_006580.3:c.22T=	NP_006571.1:p.Leu8=
NM_001378492.1:c.-93-96T=	NP_001365421.1:n.-93-96T=
NM_001378493.1:c.-93-96T=	NP_001365422.1:n.-93-96T=