Canonical Allele Identifier: CA394743713
Gene: PRM1 HGNC NCBI
RMI2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.11375051A>C (hg19) chr16:g.11281194A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281194A>C , CM000678.2:g.11281194A>C GRCh38
NC_000016.9:g.11375051A>C , CM000678.1:g.11375051A>C GRCh37
NC_000016.8:g.11282552A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000312511.4:c.45T>G (PRM1) MANE Select ENSP00000310515.3:p.Tyr15Ter
ENST00000649869.1:n.152+31416A>C (RMI2)
ENST00000312511.3:c.45T>G (PRM1) ENSP00000310515.3:p.Tyr15Ter
ENST00000572173.1:c.-515-14022A>C (RMI2) ENSP00000461206.1:n.-515-14022A>C
ENST00000573910.1:n.160+31416A>C (RMI2)
NM_002761.2:c.45T>G (PRM1) NP_002752.1:p.Tyr15Ter
XR_933070.1:n.733+31416A>C
XR_933070.3:n.876+31416A>C
NM_002761.3:c.45T>G (PRM1) MANE Select NP_002752.1:p.Tyr15Ter
Search 100 bp 5'
Search 100 bp 3'