Canonical Allele Identifier: CA1428756719

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402160G= , CM000665.2:g.190402160G=	GRCh38
NC_000003.11:g.190119949G= , CM000665.1:g.190119949G=	GRCh37
NC_000003.10:g.191602643G=	NCBI36
NG_008149.1:g.19109G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-177G= MANE Select	ENSP00000264734.3:n.115-177G=
ENST00000456423.2:c.115-7743G=	ENSP00000414136.2:n.115-7743G=
ENST00000264734.2:c.325-177G=	ENSP00000264734.2:n.325-177G=
ENST00000456423.1:c.325-7743G=	ENSP00000414136.1:n.325-7743G=
ENST00000468220.1:n.307-177G=
NM_006580.3:c.325-177G=	NP_006571.1:n.325-177G=
NM_001378492.1:c.115-177G=	NP_001365421.1:n.115-177G=
NM_001378493.1:c.115-177G=	NP_001365422.1:n.115-177G=
NM_006580.4:c.115-177G= MANE Select	NP_006571.2:n.115-177G=