Canonical Allele Identifier: CA342587710

Gene: RPS27

Linked Data

• MyVariant Identifiers: chr1:g.153963684G>C (hg19) ; chr1:g.153991208G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991208G>C , CM000663.2:g.153991208G>C	GRCh38
NC_000001.10:g.153963684G>C , CM000663.1:g.153963684G>C	GRCh37
NC_000001.9:g.152230308G>C	NCBI36
NG_053102.2:g.5454G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000477151.2:n.288G>C
ENST00000643794.1:c.221G>C	ENSP00000495765.1:p.Gly74Ala
ENST00000651669.1:c.100G>C MANE Select	ENSP00000499044.1:p.Asp34His
ENST00000368567.4:c.100G>C	ENSP00000357555.4:p.Asp34His
ENST00000392558.4:c.100G>C	ENSP00000376341.4:p.Asp34His
ENST00000477151.1:n.255G>C
ENST00000493224.5:n.366G>C
NM_001030.4:c.100G>C	NP_001021.1:p.Asp34His
NM_001030.6:c.100G>C MANE Select	NP_001021.1:p.Asp34His
NM_001349946.1:c.4G>C	NP_001336875.1:p.Asp2His
NM_001349947.1:c.4G>C	NP_001336876.1:p.Asp2His
NM_001349946.2:c.4G>C	NP_001336875.1:p.Asp2His
NM_001349947.2:c.4G>C	NP_001336876.1:p.Asp2His