Canonical Allele Identifier: CA2805865732

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281349del , CM000678.2:g.11281349del GRCh38
NC_000016.9:g.11375206del , CM000678.1:g.11375206del GRCh37
NC_000016.8:g.11282707del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+31571del (RMI2)
ENST00000312511.3:c.-111del (PRM1) ENSP00000310515.3:n.-111del
ENST00000572173.1:c.-515-13867del (RMI2) ENSP00000461206.1:n.-515-13867del
ENST00000573910.1:n.160+31571del (RMI2)
XR_933070.1:n.733+31571del
XR_933070.3:n.876+31571del