Canonical Allele Identifier: CA1428775632

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388162T= , CM000665.2:g.190388162T=	GRCh38
NC_000003.11:g.190105951T= , CM000665.1:g.190105951T=	GRCh37
NC_000003.10:g.191588645T=	NCBI36
NG_008149.1:g.5111T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-168T=	ENSP00000414136.2:n.-168T=
ENST00000264734.2:c.43T=	ENSP00000264734.2:p.Tyr15=
ENST00000456423.1:c.43T=	ENSP00000414136.1:p.Tyr15=
ENST00000468220.1:n.306+13559T=
NM_006580.3:c.43T=	NP_006571.1:p.Tyr15=
NM_001378492.1:c.-93-75T=	NP_001365421.1:n.-93-75T=
NM_001378493.1:c.-93-75T=	NP_001365422.1:n.-93-75T=