Canonical Allele Identifier: CA2631746043

Gene: PRM1 RMI2

Linked Data

• gnomAD v4: 16-11281134-TCTCCTCCGTGTCTGGCAGCTCCGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281140_11281163del , CM000678.2:g.11281140_11281163del	GRCh38
NC_000016.9:g.11374997_11375020del , CM000678.1:g.11374997_11375020del	GRCh37
NC_000016.8:g.11282498_11282521del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000312511.4:c.81_104del (PRM1) MANE Select	ENSP00000310515.3:p.Arg28_Arg35del
ENST00000649869.1:n.152+31362_152+31385del (RMI2)
ENST00000312511.3:c.81_104del (PRM1)	ENSP00000310515.3:p.Arg28_Arg35del
ENST00000572173.1:c.-515-14076_-515-14053del (RMI2)	ENSP00000461206.1:n.-515-14076_-515-14053...
ENST00000573910.1:n.160+31362_160+31385del (RMI2)
NM_002761.2:c.81_104del (PRM1)	NP_002752.1:p.Arg28_Arg35del
XR_933070.1:n.733+31362_733+31385del
XR_933070.3:n.876+31362_876+31385del
NM_002761.3:c.81_104del (PRM1) MANE Select	NP_002752.1:p.Arg28_Arg35del