Canonical Allele Identifier: CA1428775604

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388147A= , CM000665.2:g.190388147A=	GRCh38
NC_000003.11:g.190105936A= , CM000665.1:g.190105936A=	GRCh37
NC_000003.10:g.191588630A=	NCBI36
NG_008149.1:g.5096A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456423.2:c.-183A=	ENSP00000414136.2:n.-183A=
ENST00000264734.2:c.28A=	ENSP00000264734.2:p.Thr10=
ENST00000456423.1:c.28A=	ENSP00000414136.1:p.Thr10=
ENST00000468220.1:n.306+13544A=
NM_006580.3:c.28A=	NP_006571.1:p.Thr10=
NM_001378492.1:c.-93-90A=	NP_001365421.1:n.-93-90A=
NM_001378493.1:c.-93-90A=	NP_001365422.1:n.-93-90A=