Canonical Allele Identifier: CA2788644683
Gene: RPS24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78034181_78034182insACAC , CM000672.2:g.78034181_78034182insACAC GRCh38
NC_000010.10:g.79793939_79793940insACAC , CM000672.1:g.79793939_79793940insACAC GRCh37
NC_000010.9:g.79463945_79463946insACAC NCBI36
NG_012633.1:g.5422_5423insACAC
NG_029648.1:g.359_360insGTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360830.9:c.3+277_3+278insACAC ENSP00000354074.5:n.3+277_3+278insACAC
ENST00000372360.9:c.3+277_3+278insACAC MANE Select ENSP00000361435.4:n.3+277_3+278insACAC
ENST00000440692.6:c.3+277_3+278insACAC ENSP00000414321.1:n.3+277_3+278insACAC
ENST00000464716.6:c.3+277_3+278insACAC ENSP00000494231.1:n.3+277_3+278insACAC
ENST00000465692.2:n.14+277_14+278insACAC
ENST00000466129.6:n.19+277_19+278insACAC
ENST00000475468.6:n.278_279insACAC
ENST00000476545.6:c.3+277_3+278insACAC ENSP00000494169.1:n.3+277_3+278insACAC
ENST00000478655.6:n.42+277_42+278insACAC
ENST00000485708.7:n.42+277_42+278insACAC
ENST00000613865.5:c.3+277_3+278insACAC ENSP00000478869.2:n.3+277_3+278insACAC
ENST00000645440.1:c.3+277_3+278insACAC ENSP00000496738.1:n.3+277_3+278insACAC
ENST00000645698.1:n.31+277_31+278insACAC
ENST00000360830.8:c.3+277_3+278insACAC ENSP00000354074.4:n.3+277_3+278insACAC
ENST00000372360.7:c.3+277_3+278insACAC ENSP00000361435.3:n.3+277_3+278insACAC
ENST00000435275.5:c.3+277_3+278insACAC ENSP00000415549.1:n.3+277_3+278insACAC
ENST00000440692.5:c.3+277_3+278insACAC ENSP00000414321.1:n.3+277_3+278insACAC
ENST00000464716.5:n.31+277_31+278insACAC
ENST00000466129.5:n.19+277_19+278insACAC
ENST00000475468.5:n.278_279insACAC
ENST00000476545.5:n.27+277_27+278insACAC
ENST00000478655.5:n.42+277_42+278insACAC
ENST00000482069.5:n.70+195_70+196insACAC
ENST00000485708.6:n.61+277_61+278insACAC
ENST00000613865.4:c.3+277_3+278insACAC ENSP00000478869.1:n.3+277_3+278insACAC
NM_001026.4:c.3+277_3+278insACAC NP_001017.1:n.3+277_3+278insACAC
NM_001142282.1:c.3+277_3+278insACAC NP_001135754.1:n.3+277_3+278insACAC
NM_001142283.1:c.3+277_3+278insACAC NP_001135755.1:n.3+277_3+278insACAC
NM_001142284.1:c.3+277_3+278insACAC NP_001135756.1:n.3+277_3+278insACAC
NM_001142285.1:c.3+277_3+278insACAC NP_001135757.1:n.3+277_3+278insACAC
NM_033022.3:c.3+277_3+278insACAC NP_148982.1:n.3+277_3+278insACAC
NM_001142285.2:c.3+277_3+278insACAC NP_001135757.1:n.3+277_3+278insACAC
NM_033022.4:c.3+277_3+278insACAC MANE Select NP_148982.1:n.3+277_3+278insACAC
NM_001026.5:c.3+277_3+278insACAC NP_001017.1:n.3+277_3+278insACAC
NM_001142282.2:c.3+277_3+278insACAC NP_001135754.1:n.3+277_3+278insACAC
NM_001142283.2:c.3+277_3+278insACAC NP_001135755.1:n.3+277_3+278insACAC
NM_001142284.2:c.3+277_3+278insACAC NP_001135756.1:n.3+277_3+278insACAC