Canonical Allele Identifier: CA418788748

Linked Data

MyVariant Identifiers: chr1:g.93299014A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833457A>C , CM000663.2:g.92833457A>C GRCh38
NC_000001.10:g.93299014A>C , CM000663.1:g.93299014A>C GRCh37
NC_000001.9:g.93071602A>C NCBI36
NG_011779.1:g.6421A>C
NG_033051.1:g.133066T>G
NG_011779.2:g.6472A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.72A>C (RPL5) MANE Select ENSP00000359345.2:p.Arg24=
ENST00000645119.1:c.72A>C (RPL5) ENSP00000493811.1:p.Arg24=
ENST00000645300.1:c.-77-88A>C (RPL5) ENSP00000495589.1:n.-77-88A>C
ENST00000646852.1:n.101A>C (RPL5)
ENST00000315741.5:c.-79A>C (RPL5) ENSP00000359338.2:n.-79A>C
ENST00000370321.7:c.72A>C (RPL5) ENSP00000359345.2:p.Arg24=
ENST00000461952.1:n.696A>C (RPL5)
ENST00000470843.5:c.72A>C (RPL5) ENSP00000473675.1:p.Arg24=
ENST00000615519.4:c.475-423T>G (DIPK1A) ENSP00000483279.1:n.475-423T>G
NM_000969.3:c.72A>C (RPL5) NP_000960.2:p.Arg24=
NM_001252273.1:c.475-423T>G (DIPK1A) NP_001239202.1:n.475-423T>G
NM_000969.5:c.72A>C (RPL5) MANE Select NP_000960.2:p.Arg24=
NR_146333.1:n.201A>C (RPL5)
NM_001252273.2:c.475-423T>G (DIPK1A) NP_001239202.1:n.475-423T>G