Canonical Allele Identifier: CA1439212659
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578043_12578045delinsAAT , CM000666.2:g.12578043_12578045delinsAAT GRCh38
NC_000004.11:g.12579667_12579669delinsAAT , CM000666.1:g.12579667_12579669delinsAAT GRCh37
NC_000004.10:g.12188765_12188767delinsAAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31297_106+31299delinsATT
XR_001741374.1:n.254+44610_254+44612delinsATT
XR_925406.3:n.140+31297_140+31299delinsATT