Canonical Allele Identifier: CA2631746334

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281318C>G , CM000678.2:g.11281318C>G GRCh38
NC_000016.9:g.11375175C>G , CM000678.1:g.11375175C>G GRCh37
NC_000016.8:g.11282676C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000312511.4:c.-80G>C (PRM1) MANE Select ENSP00000310515.3:n.-80G>C
ENST00000649869.1:n.152+31540C>G (RMI2)
ENST00000312511.3:c.-80G>C (PRM1) ENSP00000310515.3:n.-80G>C
ENST00000572173.1:c.-515-13898C>G (RMI2) ENSP00000461206.1:n.-515-13898C>G
ENST00000573910.1:n.160+31540C>G (RMI2)
NM_002761.2:c.-80G>C (PRM1) NP_002752.1:n.-80G>C
XR_933070.1:n.733+31540C>G
XR_933070.3:n.876+31540C>G
NM_002761.3:c.-80G>C (PRM1) MANE Select NP_002752.1:n.-80G>C