Canonical Allele Identifier: CA930216604

Gene: RPS24

Linked Data

• gnomAD v3: 10-78037298-C-CAAAAAAAAAA
• gnomAD v4: 10-78037298-C-CAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78037303_78037304insAAAAAAAAAA , CM000672.2:g.78037303_78037304insAAAAAAAAAA	GRCh38
NC_000010.10:g.79797061_79797062insAAAAAAAAAA , CM000672.1:g.79797061_79797062insAAAAAAAAAA	GRCh37
NC_000010.9:g.79467067_79467068insAAAAAAAAAA	NCBI36
NG_012633.1:g.8544_8545insAAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.389_390insAAAAAAAAAA	ENSP00000354074.5:p.Ter132LysextTer?
ENST00000372360.9:c.389_390insAAAAAAAAAA MANE Select	ENSP00000361435.4:p.Ter131LysextTer33
ENST00000440692.6:c.389_390insAAAAAAAAAA	ENSP00000414321.1:p.Met131LysfsTer?
ENST00000464716.6:c.389_390insAAAAAAAAAA	ENSP00000494231.1:p.Ter133LysextTer?
ENST00000465692.2:n.400_401insAAAAAAAAAA
ENST00000476545.6:c.389_390insAAAAAAAAAA	ENSP00000494169.1:p.Ala131LysfsTer?
ENST00000478655.6:n.428_429insAAAAAAAAAA
ENST00000485708.7:n.428_429insAAAAAAAAAA
ENST00000613865.5:c.389_390insAAAAAAAAAA	ENSP00000478869.2:p.Pro131LysfsTer12
ENST00000645195.1:c.265_266insAAAAAAAAAA
ENST00000645440.1:c.389_390insAAAAAAAAAA	ENSP00000496738.1:p.Ter132LysextTer?
ENST00000645698.1:n.417_418insAAAAAAAAAA
ENST00000360830.8:c.389_390insAAAAAAAAAA	ENSP00000354074.4:p.Ter131LysextTer33
ENST00000372360.7:c.389_390insAAAAAAAAAA	ENSP00000361435.3:p.Pro131LysfsTer12
ENST00000435275.5:c.389_390insAAAAAAAAAA	ENSP00000415549.1:p.Gln131LysfsTer?
ENST00000440692.5:c.389_390insAAAAAAAAAA	ENSP00000414321.1:p.Met131LysfsTer?
ENST00000464716.5:n.417_418insAAAAAAAAAA
ENST00000465692.1:n.386_387insAAAAAAAAAA
ENST00000476545.5:n.413_414insAAAAAAAAAA
ENST00000478655.5:n.428_429insAAAAAAAAAA
ENST00000482069.5:n.456_457insAAAAAAAAAA
ENST00000485708.6:n.447_448insAAAAAAAAAA
ENST00000613865.4:c.389_390insAAAAAAAAAA	ENSP00000478869.1:p.Arg132LysfsTer?
NM_001026.4:c.389_390insAAAAAAAAAA	NP_001017.1:p.Pro131LysfsTer12
NM_001142282.1:c.389_390insAAAAAAAAAA	NP_001135754.1:p.Ter132LysextTer?
NM_001142283.1:c.389_390insAAAAAAAAAA	NP_001135755.1:p.Ter133LysextTer?
NM_001142284.1:c.389_390insAAAAAAAAAA	NP_001135756.1:p.Ter132LysextTer?
NM_001142285.1:c.389_390insAAAAAAAAAA	NP_001135757.1:p.Met131LysfsTer?
NM_033022.3:c.389_390insAAAAAAAAAA	NP_148982.1:p.Ter131LysextTer33
XM_011540034.1:c.542_543insAAAAAAAAAA	XP_011538336.1:p.Pro182LysfsTer12
XM_011540035.1:c.542_543insAAAAAAAAAA	XP_011538337.1:p.Ter184LysextTer?
XM_011540036.1:c.542_543insAAAAAAAAAA	XP_011538338.1:p.Ter183LysextTer?
XM_011540037.1:c.542_543insAAAAAAAAAA	XP_011538339.1:p.Ter183LysextTer?
XM_011540038.1:c.542_543insAAAAAAAAAA	XP_011538340.1:p.Ter182LysextTer33
NM_001142285.2:c.389_390insAAAAAAAAAA	NP_001135757.1:p.Met131LysfsTer?
NM_033022.4:c.389_390insAAAAAAAAAA MANE Select	NP_148982.1:p.Ter131LysextTer33
NM_001026.5:c.389_390insAAAAAAAAAA	NP_001017.1:p.Pro131LysfsTer12
NM_001142282.2:c.389_390insAAAAAAAAAA	NP_001135754.1:p.Ter132LysextTer?
NM_001142283.2:c.389_390insAAAAAAAAAA	NP_001135755.1:p.Ter133LysextTer?
NM_001142284.2:c.389_390insAAAAAAAAAA	NP_001135756.1:p.Ter132LysextTer?