Canonical Allele Identifier: CA418789313

Linked Data

MyVariant Identifiers: chr1:g.93303028T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837471T>A , CM000663.2:g.92837471T>A GRCh38
NC_000001.10:g.93303028T>A , CM000663.1:g.93303028T>A GRCh37
NC_000001.9:g.93075616T>A NCBI36
NG_011779.1:g.10435T>A
NG_033051.1:g.129052A>T
NG_011779.2:g.10486T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.543T>A (RPL5) MANE Select ENSP00000359345.2:p.Pro181=
ENST00000645119.1:c.324+2558T>A (RPL5) ENSP00000493811.1:n.324+2558T>A
ENST00000645300.1:c.393T>A (RPL5) ENSP00000495589.1:p.Pro131=
ENST00000645908.1:n.277T>A (RPL5)
ENST00000370321.7:c.543T>A (RPL5) ENSP00000359345.2:p.Pro181=
ENST00000497519.1:n.862T>A (RPL5)
ENST00000615519.4:c.475-4437A>T (DIPK1A) ENSP00000483279.1:n.475-4437A>T
NM_000969.3:c.543T>A (RPL5) NP_000960.2:p.Pro181=
NM_001252273.1:c.475-4437A>T (DIPK1A) NP_001239202.1:n.475-4437A>T
NM_000969.5:c.543T>A (RPL5) MANE Select NP_000960.2:p.Pro181=
NR_146333.1:n.602T>A (RPL5)
NM_001252273.2:c.475-4437A>T (DIPK1A) NP_001239202.1:n.475-4437A>T