Canonical Allele Identifier: CA2631745997

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281097C>T , CM000678.2:g.11281097C>T GRCh38
NC_000016.9:g.11374954C>T , CM000678.1:g.11374954C>T GRCh37
NC_000016.8:g.11282455C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000312511.4:c.112+30G>A (PRM1) MANE Select ENSP00000310515.3:n.112+30G>A
ENST00000649869.1:n.152+31319C>T (RMI2)
ENST00000312511.3:c.112+30G>A (PRM1) ENSP00000310515.3:n.112+30G>A
ENST00000572173.1:c.-515-14119C>T (RMI2) ENSP00000461206.1:n.-515-14119C>T
ENST00000573910.1:n.160+31319C>T (RMI2)
NM_002761.2:c.112+30G>A (PRM1) NP_002752.1:n.112+30G>A
XR_933070.1:n.733+31319C>T
XR_933070.3:n.876+31319C>T
NM_002761.3:c.112+30G>A (PRM1) MANE Select NP_002752.1:n.112+30G>A