Canonical Allele Identifier: CA2207531598
Gene: PRM1 HGNC NCBI
RMI2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281161_11281164delinsCCTT , CM000678.2:g.11281161_11281164delinsCCTT GRCh38
NC_000016.9:g.11375018_11375021delinsCCTT , CM000678.1:g.11375018_11375021delinsCCTT GRCh37
NC_000016.8:g.11282519_11282522delinsCCTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000312511.4:c.75_78delinsAAGG (PRM1) MANE Select ENSP00000310515.3:p.Arg25=
ENST00000649869.1:n.152+31383_152+31386delinsCCTT (RMI2)
ENST00000312511.3:c.75_78delinsAAGG (PRM1) ENSP00000310515.3:p.Arg25=
ENST00000572173.1:c.-515-14055_-515-14052delinsCCTT (RMI2) ENSP00000461206.1:n.-515-14055_-515-14052...
ENST00000573910.1:n.160+31383_160+31386delinsCCTT (RMI2)
NM_002761.2:c.75_78delinsAAGG (PRM1) NP_002752.1:p.Arg25=
XR_933070.1:n.733+31383_733+31386delinsCCTT
XR_933070.3:n.876+31383_876+31386delinsCCTT
NM_002761.3:c.75_78delinsAAGG (PRM1) MANE Select NP_002752.1:p.Arg25=
Search 100 bp 5'
Search 100 bp 3'