Canonical Allele Identifier: CA1420082135
Gene: CLDN11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.170776620G= , CM000665.2:g.170776620G= GRCh38
NC_000003.11:g.170494409G= , CM000665.1:g.170494409G= GRCh37
NC_000003.10:g.171977103G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000486975.1:c.*44+68426G= ENSP00000417434.1:n.*44+68426G=
XR_924701.1:n.310+4553G=
XR_924701.2:n.1210+4553G=