Canonical Allele Identifier: CA1428756731

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190402169T= , CM000665.2:g.190402169T=	GRCh38
NC_000003.11:g.190119958T= , CM000665.1:g.190119958T=	GRCh37
NC_000003.10:g.191602652T=	NCBI36
NG_008149.1:g.19118T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.3:c.115-168T= MANE Select	ENSP00000264734.3:n.115-168T=
ENST00000456423.2:c.115-7734T=	ENSP00000414136.2:n.115-7734T=
ENST00000264734.2:c.325-168T=	ENSP00000264734.2:n.325-168T=
ENST00000456423.1:c.325-7734T=	ENSP00000414136.1:n.325-7734T=
ENST00000468220.1:n.307-168T=
NM_006580.3:c.325-168T=	NP_006571.1:n.325-168T=
NM_001378492.1:c.115-168T=	NP_001365421.1:n.115-168T=
NM_001378493.1:c.115-168T=	NP_001365422.1:n.115-168T=
NM_006580.4:c.115-168T= MANE Select	NP_006571.2:n.115-168T=