Canonical Allele Identifier: CA2631745911
Gene: PRM1 HGNC NCBI
RMI2 HGNC NCBI

Linked Data

gnomAD v4: 16-11280956-CA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11280957del , CM000678.2:g.11280957del GRCh38
NC_000016.9:g.11374814del , CM000678.1:g.11374814del GRCh37
NC_000016.8:g.11282315del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000312511.4:c.*35del (PRM1) MANE Select ENSP00000310515.3:n.*35del
ENST00000649869.1:n.152+31179del (RMI2)
ENST00000312511.3:c.*35del (PRM1) ENSP00000310515.3:n.*35del
ENST00000572173.1:c.-515-14259del (RMI2) ENSP00000461206.1:n.-515-14259del
ENST00000573910.1:n.160+31179del (RMI2)
NM_002761.2:c.*35del (PRM1) NP_002752.1:n.*35del
XR_933070.1:n.733+31179del
XR_933070.3:n.876+31179del
NM_002761.3:c.*35del (PRM1) MANE Select NP_002752.1:n.*35del
Search 100 bp 5'
Search 100 bp 3'