Canonical Allele Identifier: CA1428775588

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388137A= , CM000665.2:g.190388137A=	GRCh38
NC_000003.11:g.190105926A= , CM000665.1:g.190105926A=	GRCh37
NC_000003.10:g.191588620A=	NCBI36
NG_008149.1:g.5086A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-193A=	ENSP00000414136.2:n.-193A=
ENST00000264734.2:c.18A=	ENSP00000264734.2:p.Pro6=
ENST00000456423.1:c.18A=	ENSP00000414136.1:p.Pro6=
ENST00000468220.1:n.306+13534A=
NM_006580.3:c.18A=	NP_006571.1:p.Pro6=
NM_001378492.1:c.-93-100A=	NP_001365421.1:n.-93-100A=
NM_001378493.1:c.-93-100A=	NP_001365422.1:n.-93-100A=