Canonical Allele Identifier: CA1428762736

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190408383T= , CM000665.2:g.190408383T=	GRCh38
NC_000003.11:g.190126172T= , CM000665.1:g.190126172T=	GRCh37
NC_000003.10:g.191608866T=	NCBI36
NG_008149.1:g.25332T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.452T= MANE Select	ENSP00000264734.3:p.Leu151=
ENST00000456423.2:c.115-1520T=	ENSP00000414136.2:n.115-1520T=
ENST00000264734.2:c.662T=	ENSP00000264734.2:p.Leu221=
ENST00000456423.1:c.325-1520T=	ENSP00000414136.1:n.325-1520T=
NM_006580.3:c.662T=	NP_006571.1:p.Leu221=
NM_001378492.1:c.452T=	NP_001365421.1:p.Leu151=
NM_001378493.1:c.452T=	NP_001365422.1:p.Leu151=
NM_006580.4:c.452T= MANE Select	NP_006571.2:p.Leu151=