Canonical Allele Identifier: CA2581251335

Gene: PRM1 RMI2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281309C>G , CM000678.2:g.11281309C>G	GRCh38
NC_000016.9:g.11375166C>G , CM000678.1:g.11375166C>G	GRCh37
NC_000016.8:g.11282667C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000312511.4:c.-71G>C (PRM1) MANE Select	ENSP00000310515.3:n.-71G>C
ENST00000649869.1:n.152+31531C>G (RMI2)
ENST00000312511.3:c.-71G>C (PRM1)	ENSP00000310515.3:n.-71G>C
ENST00000572173.1:c.-515-13907C>G (RMI2)	ENSP00000461206.1:n.-515-13907C>G
ENST00000573910.1:n.160+31531C>G (RMI2)
NM_002761.2:c.-71G>C (PRM1)	NP_002752.1:n.-71G>C
XR_933070.1:n.733+31531C>G
XR_933070.3:n.876+31531C>G
NM_002761.3:c.-71G>C (PRM1) MANE Select	NP_002752.1:n.-71G>C