Canonical Allele Identifier: CA1426720592
Gene: NMRAL2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185969009_185969010delinsTG , CM000665.2:g.185969009_185969010delinsTG GRCh38
NC_000003.11:g.185686798_185686799delinsTG , CM000665.1:g.185686798_185686799delinsTG GRCh37
NC_000003.10:g.187169492_187169493delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306399.3:n.270+301_270+302delinsTG
ENST00000416764.5:n.349+292_349+293delinsTG
ENST00000422108.5:n.288+360_288+361delinsTG
ENST00000423298.5:n.137-2606_137-2605delinsTG
ENST00000436375.5:n.342+301_342+302delinsTG
ENST00000445507.1:n.279+360_279+361delinsTG
NR_033752.2:n.349+292_349+293delinsTG
NR_151491.1:n.137-2606_137-2605delinsTG