Canonical Allele Identifier: CA418788747

Linked Data

MyVariant Identifiers: chr1:g.93299012C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833455C>A , CM000663.2:g.92833455C>A GRCh38
NC_000001.10:g.93299012C>A , CM000663.1:g.93299012C>A GRCh37
NC_000001.9:g.93071600C>A NCBI36
NG_011779.1:g.6419C>A
NG_033051.1:g.133068G>T
NG_011779.2:g.6470C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.70C>A (RPL5) MANE Select ENSP00000359345.2:p.Arg24=
ENST00000645119.1:c.70C>A (RPL5) ENSP00000493811.1:p.Arg24=
ENST00000645300.1:c.-77-90C>A (RPL5) ENSP00000495589.1:n.-77-90C>A
ENST00000646852.1:n.99C>A (RPL5)
ENST00000315741.5:c.-81C>A (RPL5) ENSP00000359338.2:n.-81C>A
ENST00000370321.7:c.70C>A (RPL5) ENSP00000359345.2:p.Arg24=
ENST00000461952.1:n.694C>A (RPL5)
ENST00000470843.5:c.70C>A (RPL5) ENSP00000473675.1:p.Arg24=
ENST00000615519.4:c.475-421G>T (DIPK1A) ENSP00000483279.1:n.475-421G>T
NM_000969.3:c.70C>A (RPL5) NP_000960.2:p.Arg24=
NM_001252273.1:c.475-421G>T (DIPK1A) NP_001239202.1:n.475-421G>T
NM_000969.5:c.70C>A (RPL5) MANE Select NP_000960.2:p.Arg24=
NR_146333.1:n.199C>A (RPL5)
NM_001252273.2:c.475-421G>T (DIPK1A) NP_001239202.1:n.475-421G>T