Canonical Allele Identifier: CA1921522377

Gene: RPS24

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033883C= , CM000672.2:g.78033883C=	GRCh38
NC_000010.10:g.79793641C= , CM000672.1:g.79793641C=	GRCh37
NC_000010.9:g.79463647C=	NCBI36
NG_012633.1:g.5124C=
NG_029648.1:g.658G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.-19C=	ENSP00000354074.5:n.-19C=
ENST00000372360.9:c.-19C= MANE Select	ENSP00000361435.4:n.-19C=
ENST00000440692.6:c.-19C=	ENSP00000414321.1:n.-19C=
ENST00000464716.6:c.-19C=	ENSP00000494231.1:n.-19C=
ENST00000476545.6:c.-19C=	ENSP00000494169.1:n.-19C=
ENST00000478655.6:n.21C=
ENST00000485708.7:n.21C=
ENST00000613865.5:c.-19C=	ENSP00000478869.2:n.-19C=
ENST00000645440.1:c.-19C=	ENSP00000496738.1:n.-19C=
ENST00000645698.1:n.10C=
ENST00000360830.8:c.-19C=	ENSP00000354074.4:n.-19C=
ENST00000372360.7:c.-19C=	ENSP00000361435.3:n.-19C=
ENST00000435275.5:c.-19C=	ENSP00000415549.1:n.-19C=
ENST00000440692.5:c.-19C=	ENSP00000414321.1:n.-19C=
ENST00000464716.5:n.10C=
ENST00000476545.5:n.6C=
ENST00000478655.5:n.21C=
ENST00000485708.6:n.40C=
ENST00000613865.4:c.-19C=	ENSP00000478869.1:n.-19C=
NM_001026.4:c.-19C=	NP_001017.1:n.-19C=
NM_001142282.1:c.-19C=	NP_001135754.1:n.-19C=
NM_001142283.1:c.-19C=	NP_001135755.1:n.-19C=
NM_001142284.1:c.-19C=	NP_001135756.1:n.-19C=
NM_001142285.1:c.-19C=	NP_001135757.1:n.-19C=
NM_033022.3:c.-19C=	NP_148982.1:n.-19C=
NM_001142285.2:c.-19C=	NP_001135757.1:n.-19C=
NM_033022.4:c.-19C= MANE Select	NP_148982.1:n.-19C=
NM_001026.5:c.-19C=	NP_001017.1:n.-19C=
NM_001142282.2:c.-19C=	NP_001135754.1:n.-19C=
NM_001142283.2:c.-19C=	NP_001135755.1:n.-19C=
NM_001142284.2:c.-19C=	NP_001135756.1:n.-19C=