Canonical Allele Identifier: CA1428756768

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402208G= , CM000665.2:g.190402208G=	GRCh38
NC_000003.11:g.190119997G= , CM000665.1:g.190119997G=	GRCh37
NC_000003.10:g.191602691G=	NCBI36
NG_008149.1:g.19157G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-129G= MANE Select	ENSP00000264734.3:n.115-129G=
ENST00000456423.2:c.115-7695G=	ENSP00000414136.2:n.115-7695G=
ENST00000264734.2:c.325-129G=	ENSP00000264734.2:n.325-129G=
ENST00000456423.1:c.325-7695G=	ENSP00000414136.1:n.325-7695G=
ENST00000468220.1:n.307-129G=
NM_006580.3:c.325-129G=	NP_006571.1:n.325-129G=
NM_001378492.1:c.115-129G=	NP_001365421.1:n.115-129G=
NM_001378493.1:c.115-129G=	NP_001365422.1:n.115-129G=
NM_006580.4:c.115-129G= MANE Select	NP_006571.2:n.115-129G=