Canonical Allele Identifier: CA1428775702

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388198G= , CM000665.2:g.190388198G=	GRCh38
NC_000003.11:g.190105987G= , CM000665.1:g.190105987G=	GRCh37
NC_000003.10:g.191588681G=	NCBI36
NG_008149.1:g.5147G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.-132G= MANE Select	ENSP00000264734.3:n.-132G=
ENST00000456423.2:c.-132G=	ENSP00000414136.2:n.-132G=
ENST00000264734.2:c.79G=	ENSP00000264734.2:p.Val27=
ENST00000456423.1:c.79G=	ENSP00000414136.1:p.Val27=
ENST00000468220.1:n.306+13595G=
NM_006580.3:c.79G=	NP_006571.1:p.Val27=
NM_001378492.1:c.-93-39G=	NP_001365421.1:n.-93-39G=
NM_001378493.1:c.-93-39G=	NP_001365422.1:n.-93-39G=
NM_006580.4:c.-132G= MANE Select	NP_006571.2:n.-132G=