Canonical Allele Identifier: CA1428775581

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388132A= , CM000665.2:g.190388132A=	GRCh38
NC_000003.11:g.190105921A= , CM000665.1:g.190105921A=	GRCh37
NC_000003.10:g.191588615A=	NCBI36
NG_008149.1:g.5081A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-198A=	ENSP00000414136.2:n.-198A=
ENST00000264734.2:c.13A=	ENSP00000264734.2:p.Thr5=
ENST00000456423.1:c.13A=	ENSP00000414136.1:p.Thr5=
ENST00000468220.1:n.306+13529A=
NM_006580.3:c.13A=	NP_006571.1:p.Thr5=
NM_001378492.1:c.-93-105A=	NP_001365421.1:n.-93-105A=
NM_001378493.1:c.-93-105A=	NP_001365422.1:n.-93-105A=