Canonical Allele Identifier: CA1760507872
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907559_5907571delinsGGGAGGAAAGGAC , CM000670.2:g.5907559_5907571delinsGGGAGGAAAGGAC GRCh38
NC_000008.10:g.5765081_5765093delinsGGGAGGAAAGGAC , CM000670.1:g.5765081_5765093delinsGGGAGGAAAGGAC GRCh37
NC_000008.9:g.5752489_5752501delinsGGGAGGAAAGGAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-7840_308-7828delinsGTCCTTTCCTCCC
XR_941375.1:n.308-7840_308-7828delinsGTCCTTTCCTCCC
XR_941376.1:n.406-7840_406-7828delinsGTCCTTTCCTCCC
XR_941377.1:n.308-7840_308-7828delinsGTCCTTTCCTCCC
XR_941378.1:n.216-7840_216-7828delinsGTCCTTTCCTCCC
XR_001745765.1:n.308-7840_308-7828delinsGTCCTTTCCTCCC
XR_001745766.1:n.406-7840_406-7828delinsGTCCTTTCCTCCC
XR_001745767.1:n.216-7840_216-7828delinsGTCCTTTCCTCCC
XR_001745768.1:n.308-7840_308-7828delinsGTCCTTTCCTCCC
XR_941374.2:n.308-7840_308-7828delinsGTCCTTTCCTCCC
XR_941375.2:n.308-7840_308-7828delinsGTCCTTTCCTCCC