Canonical Allele Identifier: CA1428756941

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402353G= , CM000665.2:g.190402353G=	GRCh38
NC_000003.11:g.190120142G= , CM000665.1:g.190120142G=	GRCh37
NC_000003.10:g.191602836G=	NCBI36
NG_008149.1:g.19302G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.131G= MANE Select	ENSP00000264734.3:p.Arg44=
ENST00000456423.2:c.115-7550G=	ENSP00000414136.2:n.115-7550G=
ENST00000264734.2:c.341G=	ENSP00000264734.2:p.Arg114=
ENST00000456423.1:c.325-7550G=	ENSP00000414136.1:n.325-7550G=
ENST00000468220.1:n.323G=
NM_006580.3:c.341G=	NP_006571.1:p.Arg114=
NM_001378492.1:c.131G=	NP_001365421.1:p.Arg44=
NM_001378493.1:c.131G=	NP_001365422.1:p.Arg44=
NM_006580.4:c.131G= MANE Select	NP_006571.2:p.Arg44=