Canonical Allele Identifier: CA2503890167

Gene: RPS24

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78034182_78034183insGGGGGGGGGG , CM000672.2:g.78034182_78034183insGGGGGGGGGG	GRCh38
NC_000010.10:g.79793940_79793941insGGGGGGGGGG , CM000672.1:g.79793940_79793941insGGGGGGGGGG	GRCh37
NC_000010.9:g.79463946_79463947insGGGGGGGGGG	NCBI36
NG_012633.1:g.5423_5424insGGGGGGGGGG
NG_029648.1:g.358_359insCCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.3+278_3+279insGGGGGGGGGG	ENSP00000354074.5:n.3+278_3+279insGGGGGGGGGG
ENST00000372360.9:c.3+278_3+279insGGGGGGGGGG MANE Select	ENSP00000361435.4:n.3+278_3+279insGGGGGGGGGG
ENST00000440692.6:c.3+278_3+279insGGGGGGGGGG	ENSP00000414321.1:n.3+278_3+279insGGGGGGGGGG
ENST00000464716.6:c.3+278_3+279insGGGGGGGGGG	ENSP00000494231.1:n.3+278_3+279insGGGGGGGGGG
ENST00000465692.2:n.14+278_14+279insGGGGGGGGGG
ENST00000466129.6:n.19+278_19+279insGGGGGGGGGG
ENST00000475468.6:n.279_280insGGGGGGGGGG
ENST00000476545.6:c.3+278_3+279insGGGGGGGGGG	ENSP00000494169.1:n.3+278_3+279insGGGGGGGGGG
ENST00000478655.6:n.42+278_42+279insGGGGGGGGGG
ENST00000485708.7:n.42+278_42+279insGGGGGGGGGG
ENST00000613865.5:c.3+278_3+279insGGGGGGGGGG	ENSP00000478869.2:n.3+278_3+279insGGGGGGGGGG
ENST00000645440.1:c.3+278_3+279insGGGGGGGGGG	ENSP00000496738.1:n.3+278_3+279insGGGGGGGGGG
ENST00000645698.1:n.31+278_31+279insGGGGGGGGGG
ENST00000360830.8:c.3+278_3+279insGGGGGGGGGG	ENSP00000354074.4:n.3+278_3+279insGGGGGGGGGG
ENST00000372360.7:c.3+278_3+279insGGGGGGGGGG	ENSP00000361435.3:n.3+278_3+279insGGGGGGGGGG
ENST00000435275.5:c.3+278_3+279insGGGGGGGGGG	ENSP00000415549.1:n.3+278_3+279insGGGGGGGGGG
ENST00000440692.5:c.3+278_3+279insGGGGGGGGGG	ENSP00000414321.1:n.3+278_3+279insGGGGGGGGGG
ENST00000464716.5:n.31+278_31+279insGGGGGGGGGG
ENST00000466129.5:n.19+278_19+279insGGGGGGGGGG
ENST00000475468.5:n.279_280insGGGGGGGGGG
ENST00000476545.5:n.27+278_27+279insGGGGGGGGGG
ENST00000478655.5:n.42+278_42+279insGGGGGGGGGG
ENST00000482069.5:n.70+196_70+197insGGGGGGGGGG
ENST00000485708.6:n.61+278_61+279insGGGGGGGGGG
ENST00000613865.4:c.3+278_3+279insGGGGGGGGGG	ENSP00000478869.1:n.3+278_3+279insGGGGGGGGGG
NM_001026.4:c.3+278_3+279insGGGGGGGGGG	NP_001017.1:n.3+278_3+279insGGGGGGGGGG
NM_001142282.1:c.3+278_3+279insGGGGGGGGGG	NP_001135754.1:n.3+278_3+279insGGGGGGGGGG
NM_001142283.1:c.3+278_3+279insGGGGGGGGGG	NP_001135755.1:n.3+278_3+279insGGGGGGGGGG
NM_001142284.1:c.3+278_3+279insGGGGGGGGGG	NP_001135756.1:n.3+278_3+279insGGGGGGGGGG
NM_001142285.1:c.3+278_3+279insGGGGGGGGGG	NP_001135757.1:n.3+278_3+279insGGGGGGGGGG
NM_033022.3:c.3+278_3+279insGGGGGGGGGG	NP_148982.1:n.3+278_3+279insGGGGGGGGGG
NM_001142285.2:c.3+278_3+279insGGGGGGGGGG	NP_001135757.1:n.3+278_3+279insGGGGGGGGGG
NM_033022.4:c.3+278_3+279insGGGGGGGGGG MANE Select	NP_148982.1:n.3+278_3+279insGGGGGGGGGG
NM_001026.5:c.3+278_3+279insGGGGGGGGGG	NP_001017.1:n.3+278_3+279insGGGGGGGGGG
NM_001142282.2:c.3+278_3+279insGGGGGGGGGG	NP_001135754.1:n.3+278_3+279insGGGGGGGGGG
NM_001142283.2:c.3+278_3+279insGGGGGGGGGG	NP_001135755.1:n.3+278_3+279insGGGGGGGGGG
NM_001142284.2:c.3+278_3+279insGGGGGGGGGG	NP_001135756.1:n.3+278_3+279insGGGGGGGGGG