Canonical Allele Identifier: CA2327233059

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.20217973_20217979delinsCCTTACA , CM000681.2:g.20217973_20217979delinsCCTTACA	GRCh38
NC_000019.9:g.20328782_20328788delinsCCTTACA , CM000681.1:g.20328782_20328788delinsCCTTACA	GRCh37
NC_000019.8:g.20189782_20189788delinsCCTTACA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_936388.1:n.619-663_619-657delinsTGTAAGG
XR_936389.1:n.502-663_502-657delinsTGTAAGG
XR_936390.1:n.511-663_511-657delinsTGTAAGG
XR_936391.1:n.514-663_514-657delinsTGTAAGG
XR_936392.1:n.514-663_514-657delinsTGTAAGG
XR_936394.1:n.41-761_41-755delinsCCTTACA
XR_001754063.2:n.1506-663_1506-657delinsTGTAAGG
XR_001754064.2:n.138-663_138-657delinsTGTAAGG
XR_001754066.1:n.3912-663_3912-657delinsTGTAAGG
XR_001754067.1:n.3912-663_3912-657delinsTGTAAGG
XR_001754068.1:n.3912-663_3912-657delinsTGTAAGG
XR_936394.2:n.41-761_41-755delinsCCTTACA
XR_936406.2:n.1411-663_1411-657delinsTGTAAGG