Canonical Allele Identifier: CA418789287

Linked Data

MyVariant Identifiers: chr1:g.93302935G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837378G>A , CM000663.2:g.92837378G>A GRCh38
NC_000001.10:g.93302935G>A , CM000663.1:g.93302935G>A GRCh37
NC_000001.9:g.93075523G>A NCBI36
NG_011779.1:g.10342G>A
NG_033051.1:g.129145C>T
NG_011779.2:g.10393G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.528-78G>A (RPL5) MANE Select ENSP00000359345.2:n.528-78G>A
ENST00000645119.1:c.324+2465G>A (RPL5) ENSP00000493811.1:n.324+2465G>A
ENST00000645300.1:c.378-78G>A (RPL5) ENSP00000495589.1:n.378-78G>A
ENST00000645908.1:n.262-78G>A (RPL5)
ENST00000315741.5:c.378-78G>A (RPL5) ENSP00000359338.2:n.378-78G>A
ENST00000370321.7:c.528-78G>A (RPL5) ENSP00000359345.2:n.528-78G>A
ENST00000497519.1:n.769G>A (RPL5)
ENST00000615519.4:c.475-4344C>T (DIPK1A) ENSP00000483279.1:n.475-4344C>T
NM_000969.3:c.528-78G>A (RPL5) NP_000960.2:n.528-78G>A
NM_001252273.1:c.475-4344C>T (DIPK1A) NP_001239202.1:n.475-4344C>T
NR_000006.8:n.90G>A (SNORD21)
NM_000969.5:c.528-78G>A (RPL5) MANE Select NP_000960.2:n.528-78G>A
NR_146333.1:n.587-78G>A (RPL5)
NM_001252273.2:c.475-4344C>T (DIPK1A) NP_001239202.1:n.475-4344C>T