Canonical Allele Identifier: CA420867035

Gene: RPS27

Linked Data

• dbSNP Id: rs1423635981
• gnomAD v3: 1-153991138-C-T
• gnomAD v4: 1-153991138-C-T
• MyVariant Identifiers: chr1:g.153963614C>T (hg19) ; chr1:g.153991138C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991138C>T , CM000663.2:g.153991138C>T	GRCh38
NC_000001.10:g.153963614C>T , CM000663.1:g.153963614C>T	GRCh37
NC_000001.9:g.152230238C>T	NCBI36
NG_053102.2:g.5384C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.218C>T
ENST00000643794.1:c.151C>T	ENSP00000495765.1:p.Leu51Phe
ENST00000651669.1:c.30C>T MANE Select	ENSP00000499044.1:p.Pro10=
ENST00000368567.4:c.30C>T	ENSP00000357555.4:p.Pro10=
ENST00000392558.4:c.30C>T	ENSP00000376341.4:p.Pro10=
ENST00000477151.1:n.185C>T
ENST00000493224.5:n.296C>T
NM_001030.4:c.30C>T	NP_001021.1:p.Pro10=
NM_001030.6:c.30C>T MANE Select	NP_001021.1:p.Pro10=
NM_001349946.1:c.-67C>T	NP_001336875.1:n.-67C>T
NM_001349947.1:c.-67C>T	NP_001336876.1:n.-67C>T
NM_001349946.2:c.-67C>T	NP_001336875.1:n.-67C>T
NM_001349947.2:c.-67C>T	NP_001336876.1:n.-67C>T