Canonical Allele Identifier: CA1921522386

Gene: RPS24

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033891A= , CM000672.2:g.78033891A=	GRCh38
NC_000010.10:g.79793649A= , CM000672.1:g.79793649A=	GRCh37
NC_000010.9:g.79463655A=	NCBI36
NG_012633.1:g.5132A=
NG_029648.1:g.650T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.-11A=	ENSP00000354074.5:n.-11A=
ENST00000372360.9:c.-11A= MANE Select	ENSP00000361435.4:n.-11A=
ENST00000440692.6:c.-11A=	ENSP00000414321.1:n.-11A=
ENST00000464716.6:c.-11A=	ENSP00000494231.1:n.-11A=
ENST00000465692.2:n.1A=
ENST00000466129.6:n.6A=
ENST00000476545.6:c.-11A=	ENSP00000494169.1:n.-11A=
ENST00000478655.6:n.29A=
ENST00000485708.7:n.29A=
ENST00000613865.5:c.-11A=	ENSP00000478869.2:n.-11A=
ENST00000645440.1:c.-11A=	ENSP00000496738.1:n.-11A=
ENST00000645698.1:n.18A=
ENST00000360830.8:c.-11A=	ENSP00000354074.4:n.-11A=
ENST00000372360.7:c.-11A=	ENSP00000361435.3:n.-11A=
ENST00000435275.5:c.-11A=	ENSP00000415549.1:n.-11A=
ENST00000440692.5:c.-11A=	ENSP00000414321.1:n.-11A=
ENST00000464716.5:n.18A=
ENST00000466129.5:n.6A=
ENST00000476545.5:n.14A=
ENST00000478655.5:n.29A=
ENST00000485708.6:n.48A=
ENST00000613865.4:c.-11A=	ENSP00000478869.1:n.-11A=
NM_001026.4:c.-11A=	NP_001017.1:n.-11A=
NM_001142282.1:c.-11A=	NP_001135754.1:n.-11A=
NM_001142283.1:c.-11A=	NP_001135755.1:n.-11A=
NM_001142284.1:c.-11A=	NP_001135756.1:n.-11A=
NM_001142285.1:c.-11A=	NP_001135757.1:n.-11A=
NM_033022.3:c.-11A=	NP_148982.1:n.-11A=
NM_001142285.2:c.-11A=	NP_001135757.1:n.-11A=
NM_033022.4:c.-11A= MANE Select	NP_148982.1:n.-11A=
NM_001026.5:c.-11A=	NP_001017.1:n.-11A=
NM_001142282.2:c.-11A=	NP_001135754.1:n.-11A=
NM_001142283.2:c.-11A=	NP_001135755.1:n.-11A=
NM_001142284.2:c.-11A=	NP_001135756.1:n.-11A=