Canonical Allele Identifier: CA418789316

Linked Data

MyVariant Identifiers: chr1:g.93303031T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837474T>A , CM000663.2:g.92837474T>A GRCh38
NC_000001.10:g.93303031T>A , CM000663.1:g.93303031T>A GRCh37
NC_000001.9:g.93075619T>A NCBI36
NG_011779.1:g.10438T>A
NG_033051.1:g.129049A>T
NG_011779.2:g.10489T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.546T>A (RPL5) MANE Select ENSP00000359345.2:p.Gly182=
ENST00000645119.1:c.324+2561T>A (RPL5) ENSP00000493811.1:n.324+2561T>A
ENST00000645300.1:c.396T>A (RPL5) ENSP00000495589.1:p.Gly132=
ENST00000645908.1:n.280T>A (RPL5)
ENST00000370321.7:c.546T>A (RPL5) ENSP00000359345.2:p.Gly182=
ENST00000497519.1:n.865T>A (RPL5)
ENST00000615519.4:c.475-4440A>T (DIPK1A) ENSP00000483279.1:n.475-4440A>T
NM_000969.3:c.546T>A (RPL5) NP_000960.2:p.Gly182=
NM_001252273.1:c.475-4440A>T (DIPK1A) NP_001239202.1:n.475-4440A>T
NM_000969.5:c.546T>A (RPL5) MANE Select NP_000960.2:p.Gly182=
NR_146333.1:n.605T>A (RPL5)
NM_001252273.2:c.475-4440A>T (DIPK1A) NP_001239202.1:n.475-4440A>T