Canonical Allele Identifier: CA1428758951

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190404431A= , CM000665.2:g.190404431A=	GRCh38
NC_000003.11:g.190122220A= , CM000665.1:g.190122220A=	GRCh37
NC_000003.10:g.191604914A=	NCBI36
NG_008149.1:g.21380A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.218-331A= MANE Select	ENSP00000264734.3:n.218-331A=
ENST00000456423.2:c.115-5472A=	ENSP00000414136.2:n.115-5472A=
ENST00000264734.2:c.428-331A=	ENSP00000264734.2:n.428-331A=
ENST00000456423.1:c.325-5472A=	ENSP00000414136.1:n.325-5472A=
ENST00000468220.1:n.410-331A=
NM_006580.3:c.428-331A=	NP_006571.1:n.428-331A=
NM_001378492.1:c.218-331A=	NP_001365421.1:n.218-331A=
NM_001378493.1:c.218-331A=	NP_001365422.1:n.218-331A=
NM_006580.4:c.218-331A= MANE Select	NP_006571.2:n.218-331A=