Canonical Allele Identifier: CA2480680238

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990814G= , CM000663.2:g.153990814G=	GRCh38
NC_000001.10:g.153963290G= , CM000663.1:g.153963290G=	GRCh37
NC_000001.9:g.152229914G=	NCBI36
NG_053102.2:g.5060G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.6+12G=	ENSP00000495765.1:n.6+12G=
ENST00000651669.1:c.6+12G= MANE Select	ENSP00000499044.1:n.6+12G=
ENST00000368567.4:c.6+12G=	ENSP00000357555.4:n.6+12G=
ENST00000392558.4:c.6+12G=	ENSP00000376341.4:n.6+12G=
ENST00000477151.1:n.40+12G=
ENST00000493224.5:n.52G=
NM_001030.4:c.6+12G=	NP_001021.1:n.6+12G=
NM_001030.6:c.6+12G= MANE Select	NP_001021.1:n.6+12G=
NM_001349946.1:c.-212+12G=	NP_001336875.1:n.-212+12G=
NM_001349947.1:c.-311G=	NP_001336876.1:n.-311G=
NM_001349946.2:c.-212+12G=	NP_001336875.1:n.-212+12G=
NM_001349947.2:c.-311G=	NP_001336876.1:n.-311G=