Canonical Allele Identifier: CA16040510

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92834825A>T , CM000663.2:g.92834825A>T GRCh38
NC_000001.10:g.93300382A>T , CM000663.1:g.93300382A>T GRCh37
NC_000001.9:g.93072970A>T NCBI36
NG_011779.1:g.7789A>T
NG_033051.1:g.131698T>A
NG_011779.2:g.7840A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.236A>T (RPL5) MANE Select ENSP00000359345.2:p.Tyr79Phe
ENST00000645119.1:c.236A>T (RPL5) ENSP00000493811.1:p.Tyr79Phe
ENST00000645300.1:c.86A>T (RPL5) ENSP00000495589.1:p.Tyr29Phe
ENST00000646852.1:n.265A>T (RPL5)
ENST00000315741.5:c.86A>T (RPL5) ENSP00000359338.2:p.Tyr29Phe
ENST00000370321.7:c.236A>T (RPL5) ENSP00000359345.2:p.Tyr79Phe
ENST00000461952.1:n.946A>T (RPL5)
ENST00000470843.5:c.*198A>T (RPL5) ENSP00000473675.1:n.*198A>T
ENST00000615519.4:c.475-1791T>A (DIPK1A) ENSP00000483279.1:n.475-1791T>A
NM_000969.3:c.236A>T (RPL5) NP_000960.2:p.Tyr79Phe
NM_001252273.1:c.475-1791T>A (DIPK1A) NP_001239202.1:n.475-1791T>A
NM_000969.5:c.236A>T (RPL5) MANE Select NP_000960.2:p.Tyr79Phe
NR_146333.1:n.365A>T (RPL5)
NM_001252273.2:c.475-1791T>A (DIPK1A) NP_001239202.1:n.475-1791T>A