Canonical Allele Identifier: CA1428775719

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388214G= , CM000665.2:g.190388214G=	GRCh38
NC_000003.11:g.190106003G= , CM000665.1:g.190106003G=	GRCh37
NC_000003.10:g.191588697G=	NCBI36
NG_008149.1:g.5163G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.-116G= MANE Select	ENSP00000264734.3:n.-116G=
ENST00000456423.2:c.-116G=	ENSP00000414136.2:n.-116G=
ENST00000264734.2:c.95G=	ENSP00000264734.2:p.Arg32=
ENST00000456423.1:c.95G=	ENSP00000414136.1:p.Arg32=
ENST00000468220.1:n.306+13611G=
NM_006580.3:c.95G=	NP_006571.1:p.Arg32=
NM_001378492.1:c.-93-23G=	NP_001365421.1:n.-93-23G=
NM_001378493.1:c.-93-23G=	NP_001365422.1:n.-93-23G=
NM_006580.4:c.-116G= MANE Select	NP_006571.2:n.-116G=