Canonical Allele Identifier: CA9044458

Gene: RPS15

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1440069G>C , CM000681.2:g.1440069G>C	GRCh38
NC_000019.9:g.1440068G>C , CM000681.1:g.1440068G>C	GRCh37
NC_000019.8:g.1391068G>C	NCBI36
NG_017014.1:g.6706G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592588.7:c.140G>C MANE Select	ENSP00000467466.3:p.Arg47Pro
ENST00000233609.8:c.59G>C	ENSP00000473953.1:p.Arg20Pro
ENST00000585665.2:c.41G>C	ENSP00000466366.2:p.Arg14Pro
ENST00000586096.3:c.140G>C	ENSP00000465055.2:p.Arg47Pro
ENST00000586656.5:c.41G>C	ENSP00000475096.1:p.Arg14Pro
ENST00000586686.6:c.41G>C	ENSP00000467676.2:p.Arg14Pro
ENST00000589656.6:c.140G>C	ENSP00000467855.2:p.Arg47Pro
ENST00000591032.1:c.110G>C	ENSP00000474970.2:p.Arg37Pro
ENST00000591804.6:c.41G>C	ENSP00000474543.1:p.Arg14Pro
ENST00000592588.6:c.140G>C	ENSP00000467466.3:p.Arg47Pro
ENST00000592623.5:c.59G>C	ENSP00000474433.2:p.Arg20Pro
ENST00000592700.2:n.1272G>C
ENST00000593052.5:c.161G>C	ENSP00000466010.1:p.Arg54Pro
NM_001018.3:c.140G>C	NP_001009.1:p.Arg47Pro
NM_001018.4:c.140G>C	NP_001009.1:p.Arg47Pro
NM_001308226.1:c.161G>C	NP_001295155.1:p.Arg54Pro
NM_001018.5:c.140G>C MANE Select	NP_001009.1:p.Arg47Pro
NM_001308226.2:c.161G>C	NP_001295155.1:p.Arg54Pro