Canonical Allele Identifier: CA1428762783

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190408416T= , CM000665.2:g.190408416T=	GRCh38
NC_000003.11:g.190126205T= , CM000665.1:g.190126205T=	GRCh37
NC_000003.10:g.191608899T=	NCBI36
NG_008149.1:g.25365T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.485T= MANE Select	ENSP00000264734.3:p.Phe162=
ENST00000456423.2:c.115-1487T=	ENSP00000414136.2:n.115-1487T=
ENST00000264734.2:c.695T=	ENSP00000264734.2:p.Phe232=
ENST00000456423.1:c.325-1487T=	ENSP00000414136.1:n.325-1487T=
NM_006580.3:c.695T=	NP_006571.1:p.Phe232=
NM_001378492.1:c.485T=	NP_001365421.1:p.Phe162=
NM_001378493.1:c.485T=	NP_001365422.1:p.Phe162=
NM_006580.4:c.485T= MANE Select	NP_006571.2:p.Phe162=