Canonical Allele Identifier: CA2744584595

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833380T>G , CM000663.2:g.92833380T>G GRCh38
NC_000001.10:g.93298937T>G , CM000663.1:g.93298937T>G GRCh37
NC_000001.9:g.93071525T>G NCBI36
NG_011779.1:g.6344T>G
NG_033051.1:g.133143A>C
NG_011779.2:g.6395T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.4-9T>G (RPL5) MANE Select ENSP00000359345.2:n.4-9T>G
ENST00000645119.1:c.4-9T>G (RPL5) ENSP00000493811.1:n.4-9T>G
ENST00000645300.1:c.-77-165T>G (RPL5) ENSP00000495589.1:n.-77-165T>G
ENST00000646852.1:n.33-9T>G (RPL5)
ENST00000315741.5:c.-147-9T>G (RPL5) ENSP00000359338.2:n.-147-9T>G
ENST00000370321.7:c.4-9T>G (RPL5) ENSP00000359345.2:n.4-9T>G
ENST00000461952.1:n.619T>G (RPL5)
ENST00000470843.5:c.4-9T>G (RPL5) ENSP00000473675.1:n.4-9T>G
ENST00000615519.4:c.475-346A>C (DIPK1A) ENSP00000483279.1:n.475-346A>C
NM_000969.3:c.4-9T>G (RPL5) NP_000960.2:n.4-9T>G
NM_001252273.1:c.475-346A>C (DIPK1A) NP_001239202.1:n.475-346A>C
NM_000969.5:c.4-9T>G (RPL5) MANE Select NP_000960.2:n.4-9T>G
NR_146333.1:n.133-9T>G (RPL5)
NM_001252273.2:c.475-346A>C (DIPK1A) NP_001239202.1:n.475-346A>C