Canonical Allele Identifier: CA889550544

Gene: RPS27

Linked Data

• dbSNP Id: rs1296833068
• gnomAD v3: 1-153991021-G-C
• gnomAD v4: 1-153991021-G-C
• MyVariant Identifiers: chr1:g.153963497G>C (hg19) ; chr1:g.153991021G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991021G>C , CM000663.2:g.153991021G>C	GRCh38
NC_000001.10:g.153963497G>C , CM000663.1:g.153963497G>C	GRCh37
NC_000001.9:g.152230121G>C	NCBI36
NG_053102.2:g.5267G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.101G>C
ENST00000643794.1:c.114G>C	ENSP00000495765.1:p.Gly38=
ENST00000651669.1:c.7-94G>C MANE Select	ENSP00000499044.1:n.7-94G>C
ENST00000368567.4:c.7-94G>C	ENSP00000357555.4:n.7-94G>C
ENST00000392558.4:c.7-94G>C	ENSP00000376341.4:n.7-94G>C
ENST00000477151.1:n.148G>C
ENST00000493224.5:n.259G>C
NM_001030.4:c.7-94G>C	NP_001021.1:n.7-94G>C
NM_001030.6:c.7-94G>C MANE Select	NP_001021.1:n.7-94G>C
NM_001349946.1:c.-104G>C	NP_001336875.1:n.-104G>C
NM_001349947.1:c.-104G>C	NP_001336876.1:n.-104G>C
NM_001349946.2:c.-104G>C	NP_001336875.1:n.-104G>C
NM_001349947.2:c.-104G>C	NP_001336876.1:n.-104G>C