Canonical Allele Identifier: CA1760507513

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.5907144_5907148delinsTTCCC , CM000670.2:g.5907144_5907148delinsTTCCC	GRCh38
NC_000008.10:g.5764666_5764670delinsTTCCC , CM000670.1:g.5764666_5764670delinsTTCCC	GRCh37
NC_000008.9:g.5752074_5752078delinsTTCCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941374.1:n.308-7417_308-7413delinsGGGAA
XR_941375.1:n.308-7417_308-7413delinsGGGAA
XR_941376.1:n.406-7417_406-7413delinsGGGAA
XR_941377.1:n.308-7417_308-7413delinsGGGAA
XR_941378.1:n.216-7417_216-7413delinsGGGAA
XR_001745765.1:n.308-7417_308-7413delinsGGGAA
XR_001745766.1:n.406-7417_406-7413delinsGGGAA
XR_001745767.1:n.216-7417_216-7413delinsGGGAA
XR_001745768.1:n.308-7417_308-7413delinsGGGAA
XR_941374.2:n.308-7417_308-7413delinsGGGAA
XR_941375.2:n.308-7417_308-7413delinsGGGAA