Canonical Allele Identifier: CA2207531589

Gene: PRM1 RMI2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281141_11281142delinsCG , CM000678.2:g.11281141_11281142delinsCG	GRCh38
NC_000016.9:g.11374998_11374999delinsCG , CM000678.1:g.11374998_11374999delinsCG	GRCh37
NC_000016.8:g.11282499_11282500delinsCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312511.4:c.97_98delinsCG (PRM1) MANE Select	ENSP00000310515.3:p.Arg33=
ENST00000649869.1:n.152+31363_152+31364delinsCG (RMI2)
ENST00000312511.3:c.97_98delinsCG (PRM1)	ENSP00000310515.3:p.Arg33=
ENST00000572173.1:c.-515-14075_-515-14074delinsCG (RMI2)	ENSP00000461206.1:n.-515-14075_-515-14074delinsCG
ENST00000573910.1:n.160+31363_160+31364delinsCG (RMI2)
NM_002761.2:c.97_98delinsCG (PRM1)	NP_002752.1:p.Arg33=
XR_933070.1:n.733+31363_733+31364delinsCG
XR_933070.3:n.876+31363_876+31364delinsCG
NM_002761.3:c.97_98delinsCG (PRM1) MANE Select	NP_002752.1:p.Arg33=