Canonical Allele Identifier: CA2759869842

Gene: CLDN16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.190387938G>A , CM000665.2:g.190387938G>A	GRCh38
NC_000003.11:g.190105727G>A , CM000665.1:g.190105727G>A	GRCh37
NC_000003.10:g.191588421G>A	NCBI36
NG_008149.1:g.4887G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264734.2:c.-182G>A	ENSP00000264734.2:n.-182G>A
ENST00000468220.1:n.306+13335G>A
NM_006580.3:c.-182G>A	NP_006571.1:n.-182G>A
NM_001378492.1:c.-93-299G>A	NP_001365421.1:n.-93-299G>A
NM_001378493.1:c.-93-299G>A	NP_001365422.1:n.-93-299G>A