Canonical Allele Identifier: CA1428756759

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402201T= , CM000665.2:g.190402201T=	GRCh38
NC_000003.11:g.190119990T= , CM000665.1:g.190119990T=	GRCh37
NC_000003.10:g.191602684T=	NCBI36
NG_008149.1:g.19150T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-136T= MANE Select	ENSP00000264734.3:n.115-136T=
ENST00000456423.2:c.115-7702T=	ENSP00000414136.2:n.115-7702T=
ENST00000264734.2:c.325-136T=	ENSP00000264734.2:n.325-136T=
ENST00000456423.1:c.325-7702T=	ENSP00000414136.1:n.325-7702T=
ENST00000468220.1:n.307-136T=
NM_006580.3:c.325-136T=	NP_006571.1:n.325-136T=
NM_001378492.1:c.115-136T=	NP_001365421.1:n.115-136T=
NM_001378493.1:c.115-136T=	NP_001365422.1:n.115-136T=
NM_006580.4:c.115-136T= MANE Select	NP_006571.2:n.115-136T=