Canonical Allele Identifier: CA1428762713

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190408367C= , CM000665.2:g.190408367C=	GRCh38
NC_000003.11:g.190126156C= , CM000665.1:g.190126156C=	GRCh37
NC_000003.10:g.191608850C=	NCBI36
NG_008149.1:g.25316C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.436C= MANE Select	ENSP00000264734.3:p.Arg146=
ENST00000456423.2:c.115-1536C=	ENSP00000414136.2:n.115-1536C=
ENST00000264734.2:c.646C=	ENSP00000264734.2:p.Arg216=
ENST00000456423.1:c.325-1536C=	ENSP00000414136.1:n.325-1536C=
NM_006580.3:c.646C=	NP_006571.1:p.Arg216=
NM_001378492.1:c.436C=	NP_001365421.1:p.Arg146=
NM_001378493.1:c.436C=	NP_001365422.1:p.Arg146=
NM_006580.4:c.436C= MANE Select	NP_006571.2:p.Arg146=