Canonical Allele Identifier: CA2207531597

Gene: PRM1 RMI2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281159C= , CM000678.2:g.11281159C=	GRCh38
NC_000016.9:g.11375016C= , CM000678.1:g.11375016C=	GRCh37
NC_000016.8:g.11282517C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000312511.4:c.80G= (PRM1) MANE Select	ENSP00000310515.3:p.Arg27=
ENST00000649869.1:n.152+31381C= (RMI2)
ENST00000312511.3:c.80G= (PRM1)	ENSP00000310515.3:p.Arg27=
ENST00000572173.1:c.-515-14057C= (RMI2)	ENSP00000461206.1:n.-515-14057C=
ENST00000573910.1:n.160+31381C= (RMI2)
NM_002761.2:c.80G= (PRM1)	NP_002752.1:p.Arg27=
XR_933070.1:n.733+31381C=
XR_933070.3:n.876+31381C=
NM_002761.3:c.80G= (PRM1) MANE Select	NP_002752.1:p.Arg27=