Canonical Allele Identifier: CA2002397632
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072333_116072357delinsACTAATAGCTGCTCTTTCCTTCAGT , CM000673.2:g.116072333_116072357delinsACTAATAGCTGCTCTTTCCTTCAGT GRCh38
NC_000011.9:g.115943051_115943075delinsACTAATAGCTGCTCTTTCCTTCAGT , CM000673.1:g.115943051_115943075delinsACTAATAGCTGCTCTTTCCTTCAGT GRCh37
NC_000011.8:g.115448261_115448285delinsACTAATAGCTGCTCTTTCCTTCAGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948055.1:n.192+657_192+681delinsACTGAAGGAAAGAGCAGCTATTAGT
XR_948056.1:n.311-5152_311-5128delinsACTGAAGGAAAGAGCAGCTATTAGT
XR_948057.1:n.97+752_97+776delinsACTGAAGGAAAGAGCAGCTATTAGT
XR_001748401.1:n.192+657_192+681delinsACTGAAGGAAAGAGCAGCTATTAGT
XR_948055.2:n.192+657_192+681delinsACTGAAGGAAAGAGCAGCTATTAGT
XR_948056.2:n.314-5152_314-5128delinsACTGAAGGAAAGAGCAGCTATTAGT
XR_948057.2:n.97+752_97+776delinsACTGAAGGAAAGAGCAGCTATTAGT