Canonical Allele Identifier: CA2746171917

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991232_153991233dup , CM000663.2:g.153991232_153991233dup	GRCh38
NC_000001.10:g.153963708_153963709dup , CM000663.1:g.153963708_153963709dup	GRCh37
NC_000001.9:g.152230332_152230333dup	NCBI36
NG_053102.2:g.5478_5479dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.303+9_303+10dup
ENST00000643794.1:c.236+9_236+10dup	ENSP00000495765.1:n.236+9_236+10dup
ENST00000651669.1:c.115+9_115+10dup MANE Select	ENSP00000499044.1:n.115+9_115+10dup
ENST00000368567.4:c.115+9_115+10dup	ENSP00000357555.4:n.115+9_115+10dup
ENST00000392558.4:c.124_125dup	ENSP00000376341.4:p.Ala43ArgfsTer18
ENST00000477151.1:n.270+9_270+10dup
ENST00000493224.5:n.381+9_381+10dup
NM_001030.4:c.115+9_115+10dup	NP_001021.1:n.115+9_115+10dup
NM_001030.6:c.115+9_115+10dup MANE Select	NP_001021.1:n.115+9_115+10dup
NM_001349946.1:c.19+9_19+10dup	NP_001336875.1:n.19+9_19+10dup
NM_001349947.1:c.19+9_19+10dup	NP_001336876.1:n.19+9_19+10dup
NM_001349946.2:c.19+9_19+10dup	NP_001336875.1:n.19+9_19+10dup
NM_001349947.2:c.19+9_19+10dup	NP_001336876.1:n.19+9_19+10dup