Canonical Allele Identifier: CA1760507825
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907520_5907529delinsAGGAGAAGAG , CM000670.2:g.5907520_5907529delinsAGGAGAAGAG GRCh38
NC_000008.10:g.5765042_5765051delinsAGGAGAAGAG , CM000670.1:g.5765042_5765051delinsAGGAGAAGAG GRCh37
NC_000008.9:g.5752450_5752459delinsAGGAGAAGAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-7798_308-7789delinsCTCTTCTCCT
XR_941375.1:n.308-7798_308-7789delinsCTCTTCTCCT
XR_941376.1:n.406-7798_406-7789delinsCTCTTCTCCT
XR_941377.1:n.308-7798_308-7789delinsCTCTTCTCCT
XR_941378.1:n.216-7798_216-7789delinsCTCTTCTCCT
XR_001745765.1:n.308-7798_308-7789delinsCTCTTCTCCT
XR_001745766.1:n.406-7798_406-7789delinsCTCTTCTCCT
XR_001745767.1:n.216-7798_216-7789delinsCTCTTCTCCT
XR_001745768.1:n.308-7798_308-7789delinsCTCTTCTCCT
XR_941374.2:n.308-7798_308-7789delinsCTCTTCTCCT
XR_941375.2:n.308-7798_308-7789delinsCTCTTCTCCT