Canonical Allele Identifier: CA1428776055

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388382G= , CM000665.2:g.190388382G=	GRCh38
NC_000003.11:g.190106171G= , CM000665.1:g.190106171G=	GRCh37
NC_000003.10:g.191588865G=	NCBI36
NG_008149.1:g.5331G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.53G= MANE Select	ENSP00000264734.3:p.Gly18=
ENST00000456423.2:c.53G=	ENSP00000414136.2:p.Gly18=
ENST00000264734.2:c.263G=	ENSP00000264734.2:p.Gly88=
ENST00000456423.1:c.263G=	ENSP00000414136.1:p.Gly88=
ENST00000468220.1:n.306+13779G=
NM_006580.3:c.263G=	NP_006571.1:p.Gly88=
NM_001378492.1:c.53G=	NP_001365421.1:p.Gly18=
NM_001378493.1:c.53G=	NP_001365422.1:p.Gly18=
NM_006580.4:c.53G= MANE Select	NP_006571.2:p.Gly18=