Canonical Allele Identifier: CA1206219160

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169736965_169736966delinsTG , CM000663.2:g.169736965_169736966delinsTG GRCh38
NC_000001.10:g.169706106_169706107delinsTG , CM000663.1:g.169706106_169706107delinsTG GRCh37
NC_000001.9:g.167972730_167972731delinsTG NCBI36
NG_012124.1:g.2114_2115delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000498289.5:n.852-46846_852-46845delinsTG (FIRRM)
ENST00000609271.1:c.-201-2843_-201-2842delinsCA (SELE) ENSP00000476784.1:n.-201-2843_-201-2842delinsCA