Canonical Allele Identifier: CA2207531554
Gene: PRM1 HGNC NCBI
RMI2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281089G= , CM000678.2:g.11281089G= GRCh38
NC_000016.9:g.11374946G= , CM000678.1:g.11374946G= GRCh37
NC_000016.8:g.11282447G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000312511.4:c.112+38C= (PRM1) MANE Select ENSP00000310515.3:n.112+38C=
ENST00000649869.1:n.152+31311G= (RMI2)
ENST00000312511.3:c.112+38C= (PRM1) ENSP00000310515.3:n.112+38C=
ENST00000572173.1:c.-515-14127G= (RMI2) ENSP00000461206.1:n.-515-14127G=
ENST00000573910.1:n.160+31311G= (RMI2)
NM_002761.2:c.112+38C= (PRM1) NP_002752.1:n.112+38C=
XR_933070.1:n.733+31311G=
XR_933070.3:n.876+31311G=
NM_002761.3:c.112+38C= (PRM1) MANE Select NP_002752.1:n.112+38C=
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