Canonical Allele Identifier: CA1963413208

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.34812243_34812247delinsCCAAG , CM000673.2:g.34812243_34812247delinsCCAAG	GRCh38
NC_000011.9:g.34833790_34833794delinsCCAAG , CM000673.1:g.34833790_34833794delinsCCAAG	GRCh37
NC_000011.8:g.34790366_34790370delinsCCAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_428897.2:n.579+57636_579+57640delinsCCAAG
XR_931188.1:n.693+57636_693+57640delinsCCAAG
XR_931189.1:n.854+57636_854+57640delinsCCAAG
XR_931190.1:n.639+57636_639+57640delinsCCAAG
XR_931191.1:n.689+57636_689+57640delinsCCAAG
XR_001748174.1:n.855+57636_855+57640delinsCCAAG
XR_001748176.1:n.1016+57636_1016+57640delinsCCAAG
XR_002957246.1:n.639+57636_639+57640delinsCCAAG