Canonical Allele Identifier: CA1428775579

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388131G= , CM000665.2:g.190388131G=	GRCh38
NC_000003.11:g.190105920G= , CM000665.1:g.190105920G=	GRCh37
NC_000003.10:g.191588614G=	NCBI36
NG_008149.1:g.5080G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-199G=	ENSP00000414136.2:n.-199G=
ENST00000264734.2:c.12G=	ENSP00000264734.2:p.Arg4=
ENST00000456423.1:c.12G=	ENSP00000414136.1:p.Arg4=
ENST00000468220.1:n.306+13528G=
NM_006580.3:c.12G=	NP_006571.1:p.Arg4=
NM_001378492.1:c.-93-106G=	NP_001365421.1:n.-93-106G=
NM_001378493.1:c.-93-106G=	NP_001365422.1:n.-93-106G=