Canonical Allele Identifier: CA2320058026
Gene: RPL36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5691564G= , CM000681.2:g.5691564G= GRCh38
NC_000019.9:g.5691575G= , CM000681.1:g.5691575G= GRCh37
NC_000019.8:g.5642575G= NCBI36
NG_017015.1:g.6304G=
NG_033142.1:g.33889C=

Transcript Alleles

HGVS Amino-acid change
ENST00000347512.8:c.261G= MANE Select ENSP00000252543.3:p.Arg87=
ENST00000347512.7:c.261G= ENSP00000252543.3:p.Arg87=
ENST00000394580.2:c.261G= ENSP00000378081.2:p.Arg87=
ENST00000577222.5:c.261G= ENSP00000464342.1:p.Arg87=
ENST00000579446.1:c.*54G= ENSP00000464613.1:n.*54G=
ENST00000579649.5:c.261G= ENSP00000462609.1:p.Arg87=
NM_015414.3:c.261G= NP_056229.2:p.Arg87=
NM_033643.2:c.261G= NP_378669.1:p.Arg87=
NM_033643.3:c.261G= MANE Select NP_378669.1:p.Arg87=
NM_015414.4:c.261G= NP_056229.2:p.Arg87=