Canonical Allele Identifier: CA2480680512

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991346A= , CM000663.2:g.153991346A=	GRCh38
NC_000001.10:g.153963822A= , CM000663.1:g.153963822A=	GRCh37
NC_000001.9:g.152230446A=	NCBI36
NG_053102.2:g.5592A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.303+123A=
ENST00000643794.1:c.236+123A=	ENSP00000495765.1:n.236+123A=
ENST00000651669.1:c.115+123A= MANE Select	ENSP00000499044.1:n.115+123A=
ENST00000368567.4:c.115+123A=	ENSP00000357555.4:n.115+123A=
ENST00000392558.4:c.*37A=	ENSP00000376341.4:n.*37A=
ENST00000477151.1:n.270+123A=
ENST00000493224.5:n.381+123A=
NM_001030.4:c.115+123A=	NP_001021.1:n.115+123A=
NM_001030.6:c.115+123A= MANE Select	NP_001021.1:n.115+123A=
NM_001349946.1:c.19+123A=	NP_001336875.1:n.19+123A=
NM_001349947.1:c.19+123A=	NP_001336876.1:n.19+123A=
NM_001349946.2:c.19+123A=	NP_001336875.1:n.19+123A=
NM_001349947.2:c.19+123A=	NP_001336876.1:n.19+123A=