Canonical Allele Identifier: CA2574592242

Gene: RPS24

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78037300_78037301insCC , CM000672.2:g.78037300_78037301insCC	GRCh38
NC_000010.10:g.79797058_79797059insCC , CM000672.1:g.79797058_79797059insCC	GRCh37
NC_000010.9:g.79467064_79467065insCC	NCBI36
NG_012633.1:g.8541_8542insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.386_387insCC	ENSP00000354074.5:p.Lys129AsnfsTer15
ENST00000372360.9:c.386_387insCC MANE Select	ENSP00000361435.4:p.Lys129AsnfsTer14
ENST00000440692.6:c.386_387insCC	ENSP00000414321.1:p.Lys129AsnfsTer4
ENST00000464716.6:c.386_387insCC	ENSP00000494231.1:p.Lys129AsnfsTer21
ENST00000465692.2:n.397_398insCC
ENST00000476545.6:c.386_387insCC	ENSP00000494169.1:p.Lys129AsnfsTer?
ENST00000478655.6:n.425_426insCC
ENST00000485708.7:n.425_426insCC
ENST00000613865.5:c.386_387insCC	ENSP00000478869.2:p.Lys129AsnfsTer25
ENST00000645195.1:c.262_263insCC
ENST00000645440.1:c.386_387insCC	ENSP00000496738.1:p.Lys129AsnfsTer20
ENST00000645698.1:n.414_415insCC
ENST00000360830.8:c.386_387insCC	ENSP00000354074.4:p.Lys129AsnfsTer14
ENST00000372360.7:c.386_387insCC	ENSP00000361435.3:p.Lys129AsnfsTer25
ENST00000435275.5:c.386_387insCC	ENSP00000415549.1:p.Lys129AsnfsTer15
ENST00000440692.5:c.386_387insCC	ENSP00000414321.1:p.Lys129AsnfsTer4
ENST00000464716.5:n.414_415insCC
ENST00000465692.1:n.383_384insCC
ENST00000476545.5:n.410_411insCC
ENST00000478655.5:n.425_426insCC
ENST00000482069.5:n.453_454insCC
ENST00000485708.6:n.444_445insCC
ENST00000613865.4:c.386_387insCC	ENSP00000478869.1:p.Lys129AsnfsTer?
NM_001026.4:c.386_387insCC	NP_001017.1:p.Lys129AsnfsTer25
NM_001142282.1:c.386_387insCC	NP_001135754.1:p.Lys129AsnfsTer15
NM_001142283.1:c.386_387insCC	NP_001135755.1:p.Lys129AsnfsTer21
NM_001142284.1:c.386_387insCC	NP_001135756.1:p.Lys129AsnfsTer20
NM_001142285.1:c.386_387insCC	NP_001135757.1:p.Lys129AsnfsTer4
NM_033022.3:c.386_387insCC	NP_148982.1:p.Lys129AsnfsTer14
XM_011540034.1:c.539_540insCC	XP_011538336.1:p.Lys180AsnfsTer25
XM_011540035.1:c.539_540insCC	XP_011538337.1:p.Lys180AsnfsTer21
XM_011540036.1:c.539_540insCC	XP_011538338.1:p.Lys180AsnfsTer15
XM_011540037.1:c.539_540insCC	XP_011538339.1:p.Lys180AsnfsTer20
XM_011540038.1:c.539_540insCC	XP_011538340.1:p.Lys180AsnfsTer14
NM_001142285.2:c.386_387insCC	NP_001135757.1:p.Lys129AsnfsTer4
NM_033022.4:c.386_387insCC MANE Select	NP_148982.1:p.Lys129AsnfsTer14
NM_001026.5:c.386_387insCC	NP_001017.1:p.Lys129AsnfsTer25
NM_001142282.2:c.386_387insCC	NP_001135754.1:p.Lys129AsnfsTer15
NM_001142283.2:c.386_387insCC	NP_001135755.1:p.Lys129AsnfsTer21
NM_001142284.2:c.386_387insCC	NP_001135756.1:p.Lys129AsnfsTer20