Canonical Allele Identifier: CA5571920

Gene: RPS24

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78035369C>T , CM000672.2:g.78035369C>T	GRCh38
NC_000010.10:g.79795127C>T , CM000672.1:g.79795127C>T	GRCh37
NC_000010.9:g.79465133C>T	NCBI36
NG_012633.1:g.6610C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_033022.4:c.21C>T MANE Select	NP_148982.1:p.Ile7=
ENST00000372360.9:c.21C>T MANE Select	ENSP00000361435.4:p.Ile7=
NM_001026.4:c.21C>T	NP_001017.1:p.Ile7=
NM_001026.5:c.21C>T	NP_001017.1:p.Ile7=
NM_001142282.1:c.21C>T	NP_001135754.1:p.Ile7=
NM_001142282.2:c.21C>T	NP_001135754.1:p.Ile7=
NM_001142283.1:c.21C>T	NP_001135755.1:p.Ile7=
NM_001142283.2:c.21C>T	NP_001135755.1:p.Ile7=
NM_001142284.1:c.21C>T	NP_001135756.1:p.Ile7=
NM_001142284.2:c.21C>T	NP_001135756.1:p.Ile7=
NM_001142285.1:c.21C>T	NP_001135757.1:p.Ile7=
NM_001142285.2:c.21C>T	NP_001135757.1:p.Ile7=
NM_033022.3:c.21C>T	NP_148982.1:p.Ile7=
ENST00000360830.8:c.21C>T	ENSP00000354074.4:p.Ile7=
ENST00000360830.9:c.21C>T	ENSP00000354074.5:p.Ile7=
ENST00000372360.7:c.21C>T	ENSP00000361435.3:p.Ile7=
ENST00000435275.5:c.21C>T	ENSP00000415549.1:p.Ile7=
ENST00000440692.5:c.21C>T	ENSP00000414321.1:p.Ile7=
ENST00000440692.6:c.21C>T	ENSP00000414321.1:p.Ile7=
ENST00000464716.5:n.49C>T
ENST00000464716.6:c.21C>T	ENSP00000494231.1:p.Ile7=
ENST00000465692.1:n.18C>T
ENST00000465692.2:n.32C>T
ENST00000466129.5:n.37C>T
ENST00000466129.6:n.37C>T
ENST00000475468.5:n.431C>T
ENST00000475468.6:n.431C>T
ENST00000476545.5:n.45C>T
ENST00000476545.6:c.21C>T	ENSP00000494169.1:p.Ile7=
ENST00000478655.5:n.60C>T
ENST00000478655.6:n.60C>T
ENST00000482069.5:n.88C>T
ENST00000485708.6:n.79C>T
ENST00000485708.7:n.60C>T
ENST00000613865.4:c.21C>T	ENSP00000478869.1:p.Ile7=
ENST00000613865.5:c.21C>T	ENSP00000478869.2:p.Ile7=
ENST00000645440.1:c.21C>T	ENSP00000496738.1:p.Ile7=
ENST00000645698.1:n.49C>T
ENST00000646254.1:n.230C>T
XM_011540034.1:c.174C>T	XP_011538336.1:p.Ile58=
XM_011540035.1:c.174C>T	XP_011538337.1:p.Ile58=
XM_011540036.1:c.174C>T	XP_011538338.1:p.Ile58=
XM_011540037.1:c.174C>T	XP_011538339.1:p.Ile58=
XM_011540038.1:c.174C>T	XP_011538340.1:p.Ile58=