Canonical Allele Identifier: CA2207531699

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281322G= , CM000678.2:g.11281322G= GRCh38
NC_000016.9:g.11375179G= , CM000678.1:g.11375179G= GRCh37
NC_000016.8:g.11282680G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000312511.4:c.-84C= (PRM1) MANE Select ENSP00000310515.3:n.-84C=
ENST00000649869.1:n.152+31544G= (RMI2)
ENST00000312511.3:c.-84C= (PRM1) ENSP00000310515.3:n.-84C=
ENST00000572173.1:c.-515-13894G= (RMI2) ENSP00000461206.1:n.-515-13894G=
ENST00000573910.1:n.160+31544G= (RMI2)
NM_002761.2:c.-84C= (PRM1) NP_002752.1:n.-84C=
XR_933070.1:n.733+31544G=
XR_933070.3:n.876+31544G=
NM_002761.3:c.-84C= (PRM1) MANE Select NP_002752.1:n.-84C=