Canonical Allele Identifier: CA418789338

Gene: RPL5 DIPK1A

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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