Canonical Allele Identifier: CA2631746274

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281291del , CM000678.2:g.11281291del GRCh38
NC_000016.9:g.11375148del , CM000678.1:g.11375148del GRCh37
NC_000016.8:g.11282649del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000312511.4:c.-53del (PRM1) MANE Select ENSP00000310515.3:n.-53del
ENST00000649869.1:n.152+31513del (RMI2)
ENST00000312511.3:c.-53del (PRM1) ENSP00000310515.3:n.-53del
ENST00000572173.1:c.-515-13925del (RMI2) ENSP00000461206.1:n.-515-13925del
ENST00000573910.1:n.160+31513del (RMI2)
NM_002761.2:c.-53del (PRM1) NP_002752.1:n.-53del
XR_933070.1:n.733+31513del
XR_933070.3:n.876+31513del
NM_002761.3:c.-53del (PRM1) MANE Select NP_002752.1:n.-53del