Canonical Allele Identifier: CA1608913643
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169442_8169445delinsCTAT , CM000668.2:g.8169442_8169445delinsCTAT GRCh38
NC_000006.11:g.8169675_8169678delinsCTAT , CM000668.1:g.8169675_8169678delinsCTAT GRCh37
NC_000006.10:g.8114674_8114677delinsCTAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11182_82+11185delinsCTAT
XR_926441.1:n.189+1522_189+1525delinsCTAT
XR_926442.1:n.82+11182_82+11185delinsCTAT
XR_926443.1:n.82+11182_82+11185delinsCTAT
XR_001743950.1:n.179+1522_179+1525delinsCTAT
XR_926440.2:n.74+11182_74+11185delinsCTAT
XR_926441.2:n.179+1522_179+1525delinsCTAT
XR_926443.2:n.83+11182_83+11185delinsCTAT