Canonical Allele Identifier: CA377326439

Gene: RPS24

Linked Data

• MyVariant Identifiers: chr10:g.79793663G>T (hg19) ; chr10:g.78033905G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033905G>T , CM000672.2:g.78033905G>T	GRCh38
NC_000010.10:g.79793663G>T , CM000672.1:g.79793663G>T	GRCh37
NC_000010.9:g.79463669G>T	NCBI36
NG_012633.1:g.5146G>T
NG_029648.1:g.636C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.3+1G>T	ENSP00000354074.5:n.3+1G>T
ENST00000372360.9:c.3+1G>T MANE Select	ENSP00000361435.4:n.3+1G>T
ENST00000440692.6:c.3+1G>T	ENSP00000414321.1:n.3+1G>T
ENST00000464716.6:c.3+1G>T	ENSP00000494231.1:n.3+1G>T
ENST00000465692.2:n.14+1G>T
ENST00000466129.6:n.19+1G>T
ENST00000475468.6:n.2G>T
ENST00000476545.6:c.3+1G>T	ENSP00000494169.1:n.3+1G>T
ENST00000478655.6:n.42+1G>T
ENST00000485708.7:n.42+1G>T
ENST00000613865.5:c.3+1G>T	ENSP00000478869.2:n.3+1G>T
ENST00000645440.1:c.3+1G>T	ENSP00000496738.1:n.3+1G>T
ENST00000645698.1:n.31+1G>T
ENST00000360830.8:c.3+1G>T	ENSP00000354074.4:n.3+1G>T
ENST00000372360.7:c.3+1G>T	ENSP00000361435.3:n.3+1G>T
ENST00000435275.5:c.3+1G>T	ENSP00000415549.1:n.3+1G>T
ENST00000440692.5:c.3+1G>T	ENSP00000414321.1:n.3+1G>T
ENST00000464716.5:n.31+1G>T
ENST00000466129.5:n.19+1G>T
ENST00000475468.5:n.2G>T
ENST00000476545.5:n.27+1G>T
ENST00000478655.5:n.42+1G>T
ENST00000485708.6:n.61+1G>T
ENST00000613865.4:c.3+1G>T	ENSP00000478869.1:n.3+1G>T
NM_001026.4:c.3+1G>T	NP_001017.1:n.3+1G>T
NM_001142282.1:c.3+1G>T	NP_001135754.1:n.3+1G>T
NM_001142283.1:c.3+1G>T	NP_001135755.1:n.3+1G>T
NM_001142284.1:c.3+1G>T	NP_001135756.1:n.3+1G>T
NM_001142285.1:c.3+1G>T	NP_001135757.1:n.3+1G>T
NM_033022.3:c.3+1G>T	NP_148982.1:n.3+1G>T
NM_001142285.2:c.3+1G>T	NP_001135757.1:n.3+1G>T
NM_033022.4:c.3+1G>T MANE Select	NP_148982.1:n.3+1G>T
NM_001026.5:c.3+1G>T	NP_001017.1:n.3+1G>T
NM_001142282.2:c.3+1G>T	NP_001135754.1:n.3+1G>T
NM_001142283.2:c.3+1G>T	NP_001135755.1:n.3+1G>T
NM_001142284.2:c.3+1G>T	NP_001135756.1:n.3+1G>T