Canonical Allele Identifier: CA1482797483
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542498_105542499delinsAG , CM000666.2:g.105542498_105542499delinsAG GRCh38
NC_000004.11:g.106463655_106463656delinsAG , CM000666.1:g.106463655_106463656delinsAG GRCh37
NC_000004.10:g.106683104_106683105delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.506_507delinsCT
XR_939039.1:n.666_667delinsCT
XR_939040.1:n.296-1023_296-1022delinsCT
XR_001741410.1:n.521_522delinsCT
XR_001741411.1:n.997_998delinsCT
XR_001741412.1:n.449+72_449+73delinsCT
XR_001741413.1:n.521_522delinsCT
XR_001741414.1:n.449+72_449+73delinsCT
XR_939038.2:n.521_522delinsCT
XR_939040.2:n.311-1023_311-1022delinsCT