Canonical Allele Identifier: CA1921522351

Gene: RPS24

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033855T= , CM000672.2:g.78033855T=	GRCh38
NC_000010.10:g.79793613T= , CM000672.1:g.79793613T=	GRCh37
NC_000010.9:g.79463619T=	NCBI36
NG_012633.1:g.5096T=
NG_029648.1:g.686A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613865.5:c.-47T=	ENSP00000478869.2:n.-47T=
ENST00000645440.1:c.-47T=	ENSP00000496738.1:n.-47T=
ENST00000435275.5:c.-47T=	ENSP00000415549.1:n.-47T=
ENST00000440692.5:c.-47T=	ENSP00000414321.1:n.-47T=
ENST00000485708.6:n.12T=
ENST00000613865.4:c.-47T=	ENSP00000478869.1:n.-47T=
NM_001026.4:c.-47T=	NP_001017.1:n.-47T=
NM_001142282.1:c.-47T=	NP_001135754.1:n.-47T=
NM_001142283.1:c.-47T=	NP_001135755.1:n.-47T=
NM_001142284.1:c.-47T=	NP_001135756.1:n.-47T=
NM_001142285.1:c.-47T=	NP_001135757.1:n.-47T=
NM_033022.3:c.-47T=	NP_148982.1:n.-47T=