Canonical Allele Identifier: CA1428775523

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190388091T= , CM000665.2:g.190388091T=	GRCh38
NC_000003.11:g.190105880T= , CM000665.1:g.190105880T=	GRCh37
NC_000003.10:g.191588574T=	NCBI36
NG_008149.1:g.5040T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.2:c.-29T=	ENSP00000264734.2:n.-29T=
ENST00000468220.1:n.306+13488T=
NM_006580.3:c.-29T=	NP_006571.1:n.-29T=
NM_001378492.1:c.-93-146T=	NP_001365421.1:n.-93-146T=
NM_001378493.1:c.-93-146T=	NP_001365422.1:n.-93-146T=