Canonical Allele Identifier: CA1428775607

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388148C= , CM000665.2:g.190388148C=	GRCh38
NC_000003.11:g.190105937C= , CM000665.1:g.190105937C=	GRCh37
NC_000003.10:g.191588631C=	NCBI36
NG_008149.1:g.5097C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-182C=	ENSP00000414136.2:n.-182C=
ENST00000264734.2:c.29C=	ENSP00000264734.2:p.Thr10=
ENST00000456423.1:c.29C=	ENSP00000414136.1:p.Thr10=
ENST00000468220.1:n.306+13545C=
NM_006580.3:c.29C=	NP_006571.1:p.Thr10=
NM_001378492.1:c.-93-89C=	NP_001365421.1:n.-93-89C=
NM_001378493.1:c.-93-89C=	NP_001365422.1:n.-93-89C=