Canonical Allele Identifier: CA342587677

Gene: RPS27

Linked Data

• MyVariant Identifiers: chr1:g.153963671T>A (hg19) ; chr1:g.153991195T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991195T>A , CM000663.2:g.153991195T>A	GRCh38
NC_000001.10:g.153963671T>A , CM000663.1:g.153963671T>A	GRCh37
NC_000001.9:g.152230295T>A	NCBI36
NG_053102.2:g.5441T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.275T>A
ENST00000643794.1:c.208T>A	ENSP00000495765.1:p.Phe70Ile
ENST00000651669.1:c.87T>A MANE Select	ENSP00000499044.1:p.Asn29Lys
ENST00000368567.4:c.87T>A	ENSP00000357555.4:p.Asn29Lys
ENST00000392558.4:c.87T>A	ENSP00000376341.4:p.Asn29Lys
ENST00000477151.1:n.242T>A
ENST00000493224.5:n.353T>A
NM_001030.4:c.87T>A	NP_001021.1:p.Asn29Lys
NM_001030.6:c.87T>A MANE Select	NP_001021.1:p.Asn29Lys
NM_001349946.1:c.-10T>A	NP_001336875.1:n.-10T>A
NM_001349947.1:c.-10T>A	NP_001336876.1:n.-10T>A
NM_001349946.2:c.-10T>A	NP_001336875.1:n.-10T>A
NM_001349947.2:c.-10T>A	NP_001336876.1:n.-10T>A