Canonical Allele Identifier: CA418789335

Linked Data

MyVariant Identifiers: chr1:g.93303070T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837513T>C , CM000663.2:g.92837513T>C GRCh38
NC_000001.10:g.93303070T>C , CM000663.1:g.93303070T>C GRCh37
NC_000001.9:g.93075658T>C NCBI36
NG_011779.1:g.10477T>C
NG_033051.1:g.129010A>G
NG_011779.2:g.10528T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.585T>C (RPL5) MANE Select ENSP00000359345.2:p.His195=
ENST00000645119.1:c.324+2600T>C (RPL5) ENSP00000493811.1:n.324+2600T>C
ENST00000645300.1:c.435T>C (RPL5) ENSP00000495589.1:p.His145=
ENST00000645908.1:n.319T>C (RPL5)
ENST00000370321.7:c.585T>C (RPL5) ENSP00000359345.2:p.His195=
ENST00000497519.1:n.904T>C (RPL5)
ENST00000615519.4:c.475-4479A>G (DIPK1A) ENSP00000483279.1:n.475-4479A>G
NM_000969.3:c.585T>C (RPL5) NP_000960.2:p.His195=
NM_001252273.1:c.475-4479A>G (DIPK1A) NP_001239202.1:n.475-4479A>G
NM_000969.5:c.585T>C (RPL5) MANE Select NP_000960.2:p.His195=
NR_146333.1:n.644T>C (RPL5)
NM_001252273.2:c.475-4479A>G (DIPK1A) NP_001239202.1:n.475-4479A>G