Canonical Allele Identifier: CA2631746329

Gene: PRM1 RMI2

Linked Data

• gnomAD v4: 16-11281316-A-AACTCTGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281317_11281324dup , CM000678.2:g.11281317_11281324dup	GRCh38
NC_000016.9:g.11375174_11375181dup , CM000678.1:g.11375174_11375181dup	GRCh37
NC_000016.8:g.11282675_11282682dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312511.4:c.-86_-79dup (PRM1) MANE Select	ENSP00000310515.3:n.-86_-79dup
ENST00000649869.1:n.152+31539_152+31546dup (RMI2)
ENST00000312511.3:c.-86_-79dup (PRM1)	ENSP00000310515.3:n.-86_-79dup
ENST00000572173.1:c.-515-13899_-515-13892dup (RMI2)	ENSP00000461206.1:n.-515-13899_-515-13892dup
ENST00000573910.1:n.160+31539_160+31546dup (RMI2)
NM_002761.2:c.-86_-79dup (PRM1)	NP_002752.1:n.-86_-79dup
XR_933070.1:n.733+31539_733+31546dup
XR_933070.3:n.876+31539_876+31546dup
NM_002761.3:c.-86_-79dup (PRM1) MANE Select	NP_002752.1:n.-86_-79dup