Canonical Allele Identifier: CA420949207

Gene: RPS27

Linked Data

• MyVariant Identifiers: chr1:g.153963686T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991210T>C , CM000663.2:g.153991210T>C	GRCh38
NC_000001.10:g.153963686T>C , CM000663.1:g.153963686T>C	GRCh37
NC_000001.9:g.152230310T>C	NCBI36
NG_053102.2:g.5456T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000477151.2:n.290T>C
ENST00000643794.1:c.223T>C	ENSP00000495765.1:p.Cys75Arg
ENST00000651669.1:c.102T>C MANE Select	ENSP00000499044.1:p.Asp34=
ENST00000368567.4:c.102T>C	ENSP00000357555.4:p.Asp34=
ENST00000392558.4:c.102T>C	ENSP00000376341.4:p.Asp34=
ENST00000477151.1:n.257T>C
ENST00000493224.5:n.368T>C
NM_001030.4:c.102T>C	NP_001021.1:p.Asp34=
NM_001030.6:c.102T>C MANE Select	NP_001021.1:p.Asp34=
NM_001349946.1:c.6T>C	NP_001336875.1:p.Asp2=
NM_001349947.1:c.6T>C	NP_001336876.1:p.Asp2=
NM_001349946.2:c.6T>C	NP_001336875.1:p.Asp2=
NM_001349947.2:c.6T>C	NP_001336876.1:p.Asp2=