Canonical Allele Identifier: CA1180932415

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833462C= , CM000663.2:g.92833462C= GRCh38
NC_000001.10:g.93299019C= , CM000663.1:g.93299019C= GRCh37
NC_000001.9:g.93071607C= NCBI36
NG_011779.1:g.6426C=
NG_033051.1:g.133061G=
NG_011779.2:g.6477C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370321.8:c.73+4C= (RPL5) MANE Select ENSP00000359345.2:n.73+4C=
ENST00000645119.1:c.73+4C= (RPL5) ENSP00000493811.1:n.73+4C=
ENST00000645300.1:c.-77-83C= (RPL5) ENSP00000495589.1:n.-77-83C=
ENST00000646852.1:n.102+4C= (RPL5)
ENST00000315741.5:c.-78+4C= (RPL5) ENSP00000359338.2:n.-78+4C=
ENST00000370321.7:c.73+4C= (RPL5) ENSP00000359345.2:n.73+4C=
ENST00000461952.1:n.701C= (RPL5)
ENST00000470843.5:c.73+4C= (RPL5) ENSP00000473675.1:n.73+4C=
ENST00000615519.4:c.475-428G= (DIPK1A) ENSP00000483279.1:n.475-428G=
NM_000969.3:c.73+4C= (RPL5) NP_000960.2:n.73+4C=
NM_001252273.1:c.475-428G= (DIPK1A) NP_001239202.1:n.475-428G=
NM_000969.5:c.73+4C= (RPL5) MANE Select NP_000960.2:n.73+4C=
NR_146333.1:n.202+4C= (RPL5)
NM_001252273.2:c.475-428G= (DIPK1A) NP_001239202.1:n.475-428G=