Canonical Allele Identifier: CA1963376013
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759411_34759414delinsAAAG , CM000673.2:g.34759411_34759414delinsAAAG GRCh38
NC_000011.9:g.34780958_34780961delinsAAAG , CM000673.1:g.34780958_34780961delinsAAAG GRCh37
NC_000011.8:g.34737534_34737537delinsAAAG NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+4804_579+4807delinsAAAG
XR_931188.1:n.693+4804_693+4807delinsAAAG
XR_931189.1:n.854+4804_854+4807delinsAAAG
XR_931190.1:n.639+4804_639+4807delinsAAAG
XR_931191.1:n.689+4804_689+4807delinsAAAG
XR_001748174.1:n.855+4804_855+4807delinsAAAG
XR_001748176.1:n.1016+4804_1016+4807delinsAAAG
XR_002957246.1:n.639+4804_639+4807delinsAAAG