Canonical Allele Identifier: CA2609827965

Gene: RPS24

Linked Data

• gnomAD v4: 10-78035252-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78035252T>C , CM000672.2:g.78035252T>C	GRCh38
NC_000010.10:g.79795010T>C , CM000672.1:g.79795010T>C	GRCh37
NC_000010.9:g.79465016T>C	NCBI36
NG_012633.1:g.6493T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360830.9:c.4-100T>C	ENSP00000354074.5:n.4-100T>C
ENST00000372360.9:c.4-100T>C MANE Select	ENSP00000361435.4:n.4-100T>C
ENST00000440692.6:c.4-100T>C	ENSP00000414321.1:n.4-100T>C
ENST00000464716.6:c.4-100T>C	ENSP00000494231.1:n.4-100T>C
ENST00000465692.2:n.15-100T>C
ENST00000466129.6:n.20-100T>C
ENST00000475468.6:n.414-100T>C
ENST00000476545.6:c.4-100T>C	ENSP00000494169.1:n.4-100T>C
ENST00000478655.6:n.43-100T>C
ENST00000485708.7:n.43-100T>C
ENST00000613865.5:c.4-100T>C	ENSP00000478869.2:n.4-100T>C
ENST00000645440.1:c.4-100T>C	ENSP00000496738.1:n.4-100T>C
ENST00000645698.1:n.32-100T>C
ENST00000646254.1:n.213-100T>C
ENST00000360830.8:c.4-100T>C	ENSP00000354074.4:n.4-100T>C
ENST00000372360.7:c.4-100T>C	ENSP00000361435.3:n.4-100T>C
ENST00000435275.5:c.4-100T>C	ENSP00000415549.1:n.4-100T>C
ENST00000440692.5:c.4-100T>C	ENSP00000414321.1:n.4-100T>C
ENST00000464716.5:n.32-100T>C
ENST00000466129.5:n.20-100T>C
ENST00000475468.5:n.414-100T>C
ENST00000476545.5:n.28-100T>C
ENST00000478655.5:n.43-100T>C
ENST00000482069.5:n.71-100T>C
ENST00000485708.6:n.62-100T>C
ENST00000613865.4:c.4-100T>C	ENSP00000478869.1:n.4-100T>C
NM_001026.4:c.4-100T>C	NP_001017.1:n.4-100T>C
NM_001142282.1:c.4-100T>C	NP_001135754.1:n.4-100T>C
NM_001142283.1:c.4-100T>C	NP_001135755.1:n.4-100T>C
NM_001142284.1:c.4-100T>C	NP_001135756.1:n.4-100T>C
NM_001142285.1:c.4-100T>C	NP_001135757.1:n.4-100T>C
NM_033022.3:c.4-100T>C	NP_148982.1:n.4-100T>C
XM_011540034.1:c.157-100T>C	XP_011538336.1:n.157-100T>C
XM_011540035.1:c.157-100T>C	XP_011538337.1:n.157-100T>C
XM_011540036.1:c.157-100T>C	XP_011538338.1:n.157-100T>C
XM_011540037.1:c.157-100T>C	XP_011538339.1:n.157-100T>C
XM_011540038.1:c.157-100T>C	XP_011538340.1:n.157-100T>C
NM_001142285.2:c.4-100T>C	NP_001135757.1:n.4-100T>C
NM_033022.4:c.4-100T>C MANE Select	NP_148982.1:n.4-100T>C
NM_001026.5:c.4-100T>C	NP_001017.1:n.4-100T>C
NM_001142282.2:c.4-100T>C	NP_001135754.1:n.4-100T>C
NM_001142283.2:c.4-100T>C	NP_001135755.1:n.4-100T>C
NM_001142284.2:c.4-100T>C	NP_001135756.1:n.4-100T>C