Canonical Allele Identifier: CA1428775993

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388353C= , CM000665.2:g.190388353C=	GRCh38
NC_000003.11:g.190106142C= , CM000665.1:g.190106142C=	GRCh37
NC_000003.10:g.191588836C=	NCBI36
NG_008149.1:g.5302C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264734.3:c.24C= MANE Select	ENSP00000264734.3:p.Ile8=
ENST00000456423.2:c.24C=	ENSP00000414136.2:p.Ile8=
ENST00000264734.2:c.234C=	ENSP00000264734.2:p.Ile78=
ENST00000456423.1:c.234C=	ENSP00000414136.1:p.Ile78=
ENST00000468220.1:n.306+13750C=
NM_006580.3:c.234C=	NP_006571.1:p.Ile78=
NM_001378492.1:c.24C=	NP_001365421.1:p.Ile8=
NM_001378493.1:c.24C=	NP_001365422.1:p.Ile8=
NM_006580.4:c.24C= MANE Select	NP_006571.2:p.Ile8=