Canonical Allele Identifier: CA1475277681

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89597981_89597982delinsCT , CM000666.2:g.89597981_89597982delinsCT	GRCh38
NC_000004.11:g.90519132_90519133delinsCT , CM000666.1:g.90519132_90519133delinsCT	GRCh37
NC_000004.10:g.90738155_90738156delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.298+10041_298+10042delinsCT
XR_938987.1:n.433-172_433-171delinsCT
XR_938988.1:n.299-172_299-171delinsCT
XR_938990.1:n.298+10041_298+10042delinsCT
XR_938991.1:n.298+10041_298+10042delinsCT
XR_938992.1:n.298+10041_298+10042delinsCT
XR_938994.1:n.643+10041_643+10042delinsCT
XR_938995.1:n.477+10041_477+10042delinsCT
XR_938996.1:n.298+10041_298+10042delinsCT
XR_938997.1:n.298+10041_298+10042delinsCT
XR_938986.2:n.323+10041_323+10042delinsCT
XR_938987.2:n.493-172_493-171delinsCT