Canonical Allele Identifier: CA418789185

Linked Data

MyVariant Identifiers: chr1:g.93302897T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837340T>G , CM000663.2:g.92837340T>G GRCh38
NC_000001.10:g.93302897T>G , CM000663.1:g.93302897T>G GRCh37
NC_000001.9:g.93075485T>G NCBI36
NG_011779.1:g.10304T>G
NG_033051.1:g.129183A>C
NG_011779.2:g.10355T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.528-116T>G (RPL5) MANE Select ENSP00000359345.2:n.528-116T>G
ENST00000645119.1:c.324+2427T>G (RPL5) ENSP00000493811.1:n.324+2427T>G
ENST00000645300.1:c.378-116T>G (RPL5) ENSP00000495589.1:n.378-116T>G
ENST00000645908.1:n.262-116T>G (RPL5)
ENST00000315741.5:c.378-116T>G (RPL5) ENSP00000359338.2:n.378-116T>G
ENST00000370321.7:c.528-116T>G (RPL5) ENSP00000359345.2:n.528-116T>G
ENST00000497519.1:n.731T>G (RPL5)
ENST00000615519.4:c.475-4306A>C (DIPK1A) ENSP00000483279.1:n.475-4306A>C
NM_000969.3:c.528-116T>G (RPL5) NP_000960.2:n.528-116T>G
NM_001252273.1:c.475-4306A>C (DIPK1A) NP_001239202.1:n.475-4306A>C
NR_000006.8:n.52T>G (SNORD21)
NM_000969.5:c.528-116T>G (RPL5) MANE Select NP_000960.2:n.528-116T>G
NR_146333.1:n.587-116T>G (RPL5)
NM_001252273.2:c.475-4306A>C (DIPK1A) NP_001239202.1:n.475-4306A>C