Canonical Allele Identifier: CA952563

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92840658dup , CM000663.2:g.92840658dup GRCh38
NC_000001.10:g.93306215dup , CM000663.1:g.93306215dup GRCh37
NC_000001.9:g.93078803dup NCBI36
NG_011779.1:g.13622dup
NG_033051.1:g.125873dup
NG_011779.2:g.13673dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.794+19dup (RPL5) MANE Select ENSP00000359345.2:n.794+19dup
ENST00000644549.1:n.115+19dup (RPL5)
ENST00000645119.1:c.413+19dup (RPL5) ENSP00000493811.1:n.413+19dup
ENST00000645300.1:c.644+19dup (RPL5) ENSP00000495589.1:n.644+19dup
ENST00000370321.7:c.794+19dup (RPL5) ENSP00000359345.2:n.794+19dup
ENST00000497519.1:n.1113+19dup (RPL5)
ENST00000615519.4:c.474+6533dup (DIPK1A) ENSP00000483279.1:n.474+6533dup
NM_000969.3:c.794+19dup (RPL5) NP_000960.2:n.794+19dup
NM_001252273.1:c.474+6533dup (DIPK1A) NP_001239202.1:n.474+6533dup
NM_000969.5:c.794+19dup (RPL5) MANE Select NP_000960.2:n.794+19dup
NR_146333.1:n.853+19dup (RPL5)
NM_001252273.2:c.474+6533dup (DIPK1A) NP_001239202.1:n.474+6533dup