Canonical Allele Identifier: CA2207531645

Gene: PRM1 RMI2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281233G= , CM000678.2:g.11281233G=	GRCh38
NC_000016.9:g.11375090G= , CM000678.1:g.11375090G=	GRCh37
NC_000016.8:g.11282591G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000312511.4:c.6C= (PRM1) MANE Select	ENSP00000310515.3:p.Ala2=
ENST00000649869.1:n.152+31455G= (RMI2)
ENST00000312511.3:c.6C= (PRM1)	ENSP00000310515.3:p.Ala2=
ENST00000572173.1:c.-515-13983G= (RMI2)	ENSP00000461206.1:n.-515-13983G=
ENST00000573910.1:n.160+31455G= (RMI2)
NM_002761.2:c.6C= (PRM1)	NP_002752.1:p.Ala2=
XR_933070.1:n.733+31455G=
XR_933070.3:n.876+31455G=
NM_002761.3:c.6C= (PRM1) MANE Select	NP_002752.1:p.Ala2=