Canonical Allele Identifier: CA2317723214

Gene: RPS15

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1440137A= , CM000681.2:g.1440137A=	GRCh38
NC_000019.9:g.1440136A= , CM000681.1:g.1440136A=	GRCh37
NC_000019.8:g.1391136A=	NCBI36
NG_017014.1:g.6774A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001018.5:c.208A= MANE Select	NP_001009.1:p.Met70=
ENST00000592588.7:c.208A= MANE Select	ENSP00000467466.3:p.Met70=
NM_001018.3:c.208A=	NP_001009.1:p.Met70=
NM_001018.4:c.208A=	NP_001009.1:p.Met70=
NM_001308226.1:c.229A=	NP_001295155.1:p.Met77=
NM_001308226.2:c.229A=	NP_001295155.1:p.Met77=
ENST00000233609.8:c.127A=	ENSP00000473953.1:p.Met43=
ENST00000585665.2:c.109A=	ENSP00000466366.2:p.Met37=
ENST00000586096.3:c.208A=	ENSP00000465055.2:p.Met70=
ENST00000586656.5:c.109A=	ENSP00000475096.1:p.Met37=
ENST00000586686.6:c.109A=	ENSP00000467676.2:p.Met37=
ENST00000589656.6:c.208A=	ENSP00000467855.2:p.Met70=
ENST00000591032.1:c.178A=	ENSP00000474970.2:p.Met60=
ENST00000591804.6:c.109A=	ENSP00000474543.1:p.Met37=
ENST00000592588.6:c.208A=	ENSP00000467466.3:p.Met70=
ENST00000592623.5:c.127A=	ENSP00000474433.2:p.Met43=
ENST00000592700.2:n.1340A=
ENST00000593052.5:c.229A=	ENSP00000466010.1:p.Met77=