Canonical Allele Identifier: CA418788746

Linked Data

MyVariant Identifiers: chr1:g.93299011A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833454A>T , CM000663.2:g.92833454A>T GRCh38
NC_000001.10:g.93299011A>T , CM000663.1:g.93299011A>T GRCh37
NC_000001.9:g.93071599A>T NCBI36
NG_011779.1:g.6418A>T
NG_033051.1:g.133069T>A
NG_011779.2:g.6469A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.69A>T (RPL5) MANE Select ENSP00000359345.2:p.Arg23=
ENST00000645119.1:c.69A>T (RPL5) ENSP00000493811.1:p.Arg23=
ENST00000645300.1:c.-77-91A>T (RPL5) ENSP00000495589.1:n.-77-91A>T
ENST00000646852.1:n.98A>T (RPL5)
ENST00000315741.5:c.-82A>T (RPL5) ENSP00000359338.2:n.-82A>T
ENST00000370321.7:c.69A>T (RPL5) ENSP00000359345.2:p.Arg23=
ENST00000461952.1:n.693A>T (RPL5)
ENST00000470843.5:c.69A>T (RPL5) ENSP00000473675.1:p.Arg23=
ENST00000615519.4:c.475-420T>A (DIPK1A) ENSP00000483279.1:n.475-420T>A
NM_000969.3:c.69A>T (RPL5) NP_000960.2:p.Arg23=
NM_001252273.1:c.475-420T>A (DIPK1A) NP_001239202.1:n.475-420T>A
NM_000969.5:c.69A>T (RPL5) MANE Select NP_000960.2:p.Arg23=
NR_146333.1:n.198A>T (RPL5)
NM_001252273.2:c.475-420T>A (DIPK1A) NP_001239202.1:n.475-420T>A