Canonical Allele Identifier: CA341243002

Gene: RPL5 DIPK1A

Linked Data

• dbSNP Id: rs1477777637
• MyVariant Identifiers: chr1:g.93303120T>A (hg19) ; chr1:g.92837563T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92837563T>A , CM000663.2:g.92837563T>A	GRCh38
NC_000001.10:g.93303120T>A , CM000663.1:g.93303120T>A	GRCh37
NC_000001.9:g.93075708T>A	NCBI36
NG_011779.1:g.10527T>A
NG_033051.1:g.128960A>T
NG_011779.2:g.10578T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370321.8:c.635T>A (RPL5) MANE Select	ENSP00000359345.2:p.Met212Lys
ENST00000645119.1:c.324+2650T>A (RPL5)	ENSP00000493811.1:n.324+2650T>A
ENST00000645300.1:c.485T>A (RPL5)	ENSP00000495589.1:p.Met162Lys
ENST00000645908.1:n.369T>A (RPL5)
ENST00000370321.7:c.635T>A (RPL5)	ENSP00000359345.2:p.Met212Lys
ENST00000497519.1:n.954T>A (RPL5)
ENST00000615519.4:c.475-4529A>T (DIPK1A)	ENSP00000483279.1:n.475-4529A>T
NM_000969.3:c.635T>A (RPL5)	NP_000960.2:p.Met212Lys
NM_001252273.1:c.475-4529A>T (DIPK1A)	NP_001239202.1:n.475-4529A>T
NM_000969.5:c.635T>A (RPL5) MANE Select	NP_000960.2:p.Met212Lys
NR_146333.1:n.694T>A (RPL5)
NM_001252273.2:c.475-4529A>T (DIPK1A)	NP_001239202.1:n.475-4529A>T