Canonical Allele Identifier: CA2480680299

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990900T= , CM000663.2:g.153990900T=	GRCh38
NC_000001.10:g.153963376T= , CM000663.1:g.153963376T=	GRCh37
NC_000001.9:g.152230000T=	NCBI36
NG_053102.2:g.5146T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.7-14T=	ENSP00000495765.1:n.7-14T=
ENST00000651669.1:c.6+98T= MANE Select	ENSP00000499044.1:n.6+98T=
ENST00000368567.4:c.6+98T=	ENSP00000357555.4:n.6+98T=
ENST00000392558.4:c.6+98T=	ENSP00000376341.4:n.6+98T=
ENST00000477151.1:n.41-14T=
ENST00000493224.5:n.138T=
NM_001030.4:c.6+98T=	NP_001021.1:n.6+98T=
NM_001030.6:c.6+98T= MANE Select	NP_001021.1:n.6+98T=
NM_001349946.1:c.-211-14T=	NP_001336875.1:n.-211-14T=
NM_001349947.1:c.-225T=	NP_001336876.1:n.-225T=
NM_001349946.2:c.-211-14T=	NP_001336875.1:n.-211-14T=
NM_001349947.2:c.-225T=	NP_001336876.1:n.-225T=