Canonical Allele Identifier: CA1941456005
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122458385_122458388delinsAAAG , CM000672.2:g.122458385_122458388delinsAAAG GRCh38
NC_000010.10:g.124217901_124217904delinsAAAG , CM000672.1:g.124217901_124217904delinsAAAG GRCh37
NC_000010.9:g.124207891_124207894delinsAAAG NCBI36
NG_011554.1:g.1861_1864delinsAAAG
NG_011725.1:g.8723_8726delinsAAAG

Transcript Alleles

HGVS Amino-acid Change
XR_946382.1:n.1827+107_1827+110delinsCTTT
XR_946383.1:n.1827+107_1827+110delinsCTTT
XR_946384.1:n.1576+107_1576+110delinsCTTT
XR_946385.1:n.1827+107_1827+110delinsCTTT
XR_946382.2:n.1855+107_1855+110delinsCTTT
XR_946383.2:n.1855+107_1855+110delinsCTTT
XR_946384.2:n.1580+107_1580+110delinsCTTT
XR_946385.2:n.1855+107_1855+110delinsCTTT