Canonical Allele Identifier: CA493605908

Gene: PRM1 RMI2

Linked Data

• MyVariant Identifiers: chr16:g.11374867C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281010C>G , CM000678.2:g.11281010C>G	GRCh38
NC_000016.9:g.11374867C>G , CM000678.1:g.11374867C>G	GRCh37
NC_000016.8:g.11282368C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312511.4:c.138G>C (PRM1) MANE Select	ENSP00000310515.3:p.Pro46=
ENST00000649869.1:n.152+31232C>G (RMI2)
ENST00000312511.3:c.138G>C (PRM1)	ENSP00000310515.3:p.Pro46=
ENST00000572173.1:c.-515-14206C>G (RMI2)	ENSP00000461206.1:n.-515-14206C>G
ENST00000573910.1:n.160+31232C>G (RMI2)
NM_002761.2:c.138G>C (PRM1)	NP_002752.1:p.Pro46=
XR_933070.1:n.733+31232C>G
XR_933070.3:n.876+31232C>G
NM_002761.3:c.138G>C (PRM1) MANE Select	NP_002752.1:p.Pro46=