Canonical Allele Identifier: CA342586886

Gene: RPS27

Linked Data

• MyVariant Identifiers: chr1:g.153963274T>C (hg19) ; chr1:g.153990798T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990798T>C , CM000663.2:g.153990798T>C	GRCh38
NC_000001.10:g.153963274T>C , CM000663.1:g.153963274T>C	GRCh37
NC_000001.9:g.152229898T>C	NCBI36
NG_053102.2:g.5044T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.2T>C	ENSP00000495765.1:p.Met1Thr
ENST00000651669.1:c.2T>C MANE Select	ENSP00000499044.1:p.Met1Thr
ENST00000368567.4:c.2T>C	ENSP00000357555.4:p.Met1Thr
ENST00000392558.4:c.2T>C	ENSP00000376341.4:p.Met1Thr
ENST00000477151.1:n.36T>C
ENST00000493224.5:n.36T>C
NM_001030.4:c.2T>C	NP_001021.1:p.Met1Thr
NM_001030.6:c.2T>C MANE Select	NP_001021.1:p.Met1Thr
NM_001349946.1:c.-216T>C	NP_001336875.1:n.-216T>C
NM_001349947.1:c.-327T>C	NP_001336876.1:n.-327T>C
NM_001349946.2:c.-216T>C	NP_001336875.1:n.-216T>C
NM_001349947.2:c.-327T>C	NP_001336876.1:n.-327T>C