Canonical Allele Identifier: CA9044436

Gene: RPS15

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1438866C>T , CM000681.2:g.1438866C>T	GRCh38
NC_000019.9:g.1438865C>T , CM000681.1:g.1438865C>T	GRCh37
NC_000019.8:g.1389865C>T	NCBI36
NG_017014.1:g.5503C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592588.7:c.63C>T MANE Select	ENSP00000467466.3:p.Asp21=
ENST00000233609.8:c.-19C>T	ENSP00000473953.1:n.-19C>T
ENST00000585665.2:c.-30C>T	ENSP00000466366.2:n.-30C>T
ENST00000586096.3:c.63C>T	ENSP00000465055.2:p.Asp21=
ENST00000586656.5:c.-148C>T	ENSP00000475096.1:n.-148C>T
ENST00000586686.6:c.-88C>T	ENSP00000467676.2:n.-88C>T
ENST00000589656.6:c.63C>T	ENSP00000467855.2:p.Asp21=
ENST00000591032.1:c.-26C>T	ENSP00000474970.2:n.-26C>T
ENST00000591804.6:c.-258C>T	ENSP00000474543.1:n.-258C>T
ENST00000592588.6:c.63C>T	ENSP00000467466.3:p.Asp21=
ENST00000592623.5:c.-19C>T	ENSP00000474433.2:n.-19C>T
ENST00000592700.2:n.69C>T
ENST00000593052.5:c.84C>T	ENSP00000466010.1:p.Asp28=
ENST00000617694.4:c.-251C>T	ENSP00000483399.1:n.-251C>T
NM_001018.3:c.63C>T	NP_001009.1:p.Asp21=
NM_001018.4:c.63C>T	NP_001009.1:p.Asp21=
NM_001308226.1:c.84C>T	NP_001295155.1:p.Asp28=
NM_001018.5:c.63C>T MANE Select	NP_001009.1:p.Asp21=
NM_001308226.2:c.84C>T	NP_001295155.1:p.Asp28=