Canonical Allele Identifier: CA1964082092
Gene: PRR5L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350012G= , CM000673.2:g.36350012G= GRCh38
NC_000011.9:g.36371562G= , CM000673.1:g.36371562G= GRCh37
NC_000011.8:g.36328138G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50985G= MANE Select ENSP00000435050.1:n.-125-50985G=
ENST00000527172.5:c.-291-43834G= ENSP00000433708.1:n.-291-43834G=
ENST00000529034.5:n.152-50985G=
ENST00000530639.5:c.-125-50985G= ENSP00000435050.1:n.-125-50985G=
ENST00000532121.5:c.-179G= ENSP00000433893.1:n.-179G=
NM_001160167.1:c.-125-50985G= NP_001153639.1:n.-125-50985G=
NM_001160167.2:c.-125-50985G= MANE Select NP_001153639.1:n.-125-50985G=
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