Canonical Allele Identifier: CA418789337

Linked Data

MyVariant Identifiers: chr1:g.93303073G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837516G>A , CM000663.2:g.92837516G>A GRCh38
NC_000001.10:g.93303073G>A , CM000663.1:g.93303073G>A GRCh37
NC_000001.9:g.93075661G>A NCBI36
NG_011779.1:g.10480G>A
NG_033051.1:g.129007C>T
NG_011779.2:g.10531G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.588G>A (RPL5) MANE Select ENSP00000359345.2:p.Arg196=
ENST00000645119.1:c.324+2603G>A (RPL5) ENSP00000493811.1:n.324+2603G>A
ENST00000645300.1:c.438G>A (RPL5) ENSP00000495589.1:p.Arg146=
ENST00000645908.1:n.322G>A (RPL5)
ENST00000370321.7:c.588G>A (RPL5) ENSP00000359345.2:p.Arg196=
ENST00000497519.1:n.907G>A (RPL5)
ENST00000615519.4:c.475-4482C>T (DIPK1A) ENSP00000483279.1:n.475-4482C>T
NM_000969.3:c.588G>A (RPL5) NP_000960.2:p.Arg196=
NM_001252273.1:c.475-4482C>T (DIPK1A) NP_001239202.1:n.475-4482C>T
NM_000969.5:c.588G>A (RPL5) MANE Select NP_000960.2:p.Arg196=
NR_146333.1:n.647G>A (RPL5)
NM_001252273.2:c.475-4482C>T (DIPK1A) NP_001239202.1:n.475-4482C>T