Canonical Allele Identifier: CA2207531644

Gene: PRM1 RMI2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281230C= , CM000678.2:g.11281230C=	GRCh38
NC_000016.9:g.11375087C= , CM000678.1:g.11375087C=	GRCh37
NC_000016.8:g.11282588C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000312511.4:c.9G= (PRM1) MANE Select	ENSP00000310515.3:p.Arg3=
ENST00000649869.1:n.152+31452C= (RMI2)
ENST00000312511.3:c.9G= (PRM1)	ENSP00000310515.3:p.Arg3=
ENST00000572173.1:c.-515-13986C= (RMI2)	ENSP00000461206.1:n.-515-13986C=
ENST00000573910.1:n.160+31452C= (RMI2)
NM_002761.2:c.9G= (PRM1)	NP_002752.1:p.Arg3=
XR_933070.1:n.733+31452C=
XR_933070.3:n.876+31452C=
NM_002761.3:c.9G= (PRM1) MANE Select	NP_002752.1:p.Arg3=