Canonical Allele Identifier: CA2631746323

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281315G>T , CM000678.2:g.11281315G>T GRCh38
NC_000016.9:g.11375172G>T , CM000678.1:g.11375172G>T GRCh37
NC_000016.8:g.11282673G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000312511.4:c.-77C>A (PRM1) MANE Select ENSP00000310515.3:n.-77C>A
ENST00000649869.1:n.152+31537G>T (RMI2)
ENST00000312511.3:c.-77C>A (PRM1) ENSP00000310515.3:n.-77C>A
ENST00000572173.1:c.-515-13901G>T (RMI2) ENSP00000461206.1:n.-515-13901G>T
ENST00000573910.1:n.160+31537G>T (RMI2)
NM_002761.2:c.-77C>A (PRM1) NP_002752.1:n.-77C>A
XR_933070.1:n.733+31537G>T
XR_933070.3:n.876+31537G>T
NM_002761.3:c.-77C>A (PRM1) MANE Select NP_002752.1:n.-77C>A