Canonical Allele Identifier: CA341242684
Community Standard Title: NM_000969.5(RPL5):c.527+1G>T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92836393G>T , CM000663.2:g.92836393G>T GRCh38
NC_000001.10:g.93301950G>T , CM000663.1:g.93301950G>T GRCh37
NC_000001.9:g.93074538G>T NCBI36
NG_011779.1:g.9357G>T
NG_033051.1:g.130130C>A
NG_011779.2:g.9408G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000969.5:c.527+1G>T (RPL5) MANE Select NP_000960.2:n.527+1G>T
ENST00000370321.8:c.527+1G>T (RPL5) MANE Select ENSP00000359345.2:n.527+1G>T
NM_000969.3:c.527+1G>T (RPL5) NP_000960.2:n.527+1G>T
NM_001252273.1:c.475-3359C>A (DIPK1A) NP_001239202.1:n.475-3359C>A
NM_001252273.2:c.475-3359C>A (DIPK1A) NP_001239202.1:n.475-3359C>A
NR_146333.1:n.586+1G>T (RPL5)
ENST00000315741.5:c.377+1G>T (RPL5) ENSP00000359338.2:n.377+1G>T
ENST00000370321.7:c.527+1G>T (RPL5) ENSP00000359345.2:n.527+1G>T
ENST00000615519.4:c.475-3359C>A (DIPK1A) ENSP00000483279.1:n.475-3359C>A
ENST00000645119.1:c.324+1480G>T (RPL5) ENSP00000493811.1:n.324+1480G>T
ENST00000645300.1:c.377+1G>T (RPL5) ENSP00000495589.1:n.377+1G>T
ENST00000645908.1:n.261+1G>T (RPL5)