Canonical Allele Identifier: CA420867153

Gene: RPS27

Linked Data

• dbSNP Id: rs1444617106
• MyVariant Identifiers: chr1:g.153963641C>T (hg19) ; chr1:g.153991165C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991165C>T , CM000663.2:g.153991165C>T	GRCh38
NC_000001.10:g.153963641C>T , CM000663.1:g.153963641C>T	GRCh37
NC_000001.9:g.152230265C>T	NCBI36
NG_053102.2:g.5411C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.245C>T
ENST00000643794.1:c.178C>T	ENSP00000495765.1:p.Gln60Ter
ENST00000651669.1:c.57C>T MANE Select	ENSP00000499044.1:p.His19=
ENST00000368567.4:c.57C>T	ENSP00000357555.4:p.His19=
ENST00000392558.4:c.57C>T	ENSP00000376341.4:p.His19=
ENST00000477151.1:n.212C>T
ENST00000493224.5:n.323C>T
NM_001030.4:c.57C>T	NP_001021.1:p.His19=
NM_001030.6:c.57C>T MANE Select	NP_001021.1:p.His19=
NM_001349946.1:c.-40C>T	NP_001336875.1:n.-40C>T
NM_001349947.1:c.-40C>T	NP_001336876.1:n.-40C>T
NM_001349946.2:c.-40C>T	NP_001336875.1:n.-40C>T
NM_001349947.2:c.-40C>T	NP_001336876.1:n.-40C>T