Canonical Allele Identifier: CA1428775548

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388114C= , CM000665.2:g.190388114C=	GRCh38
NC_000003.11:g.190105903C= , CM000665.1:g.190105903C=	GRCh37
NC_000003.10:g.191588597C=	NCBI36
NG_008149.1:g.5063C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.2:c.-6C=	ENSP00000264734.2:n.-6C=
ENST00000468220.1:n.306+13511C=
NM_006580.3:c.-6C=	NP_006571.1:n.-6C=
NM_001378492.1:c.-93-123C=	NP_001365421.1:n.-93-123C=
NM_001378493.1:c.-93-123C=	NP_001365422.1:n.-93-123C=