Canonical Allele Identifier: CA2480680382

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991069A= , CM000663.2:g.153991069A=	GRCh38
NC_000001.10:g.153963545A= , CM000663.1:g.153963545A=	GRCh37
NC_000001.9:g.152230169A=	NCBI36
NG_053102.2:g.5315A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.149A=
ENST00000643794.1:c.127+35A=	ENSP00000495765.1:n.127+35A=
ENST00000651669.1:c.7-46A= MANE Select	ENSP00000499044.1:n.7-46A=
ENST00000368567.4:c.7-46A=	ENSP00000357555.4:n.7-46A=
ENST00000392558.4:c.7-46A=	ENSP00000376341.4:n.7-46A=
ENST00000477151.1:n.161+35A=
ENST00000493224.5:n.272+35A=
NM_001030.4:c.7-46A=	NP_001021.1:n.7-46A=
NM_001030.6:c.7-46A= MANE Select	NP_001021.1:n.7-46A=
NM_001349946.1:c.-91+35A=	NP_001336875.1:n.-91+35A=
NM_001349947.1:c.-91+35A=	NP_001336876.1:n.-91+35A=
NM_001349946.2:c.-91+35A=	NP_001336875.1:n.-91+35A=
NM_001349947.2:c.-91+35A=	NP_001336876.1:n.-91+35A=