Canonical Allele Identifier: CA2648114000

Gene: RPS27

Linked Data

• gnomAD v4: 1-153991008-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991008G>T , CM000663.2:g.153991008G>T	GRCh38
NC_000001.10:g.153963484G>T , CM000663.1:g.153963484G>T	GRCh37
NC_000001.9:g.152230108G>T	NCBI36
NG_053102.2:g.5254G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.88G>T
ENST00000643794.1:c.101G>T	ENSP00000495765.1:p.Arg34Met
ENST00000651669.1:c.7-107G>T MANE Select	ENSP00000499044.1:n.7-107G>T
ENST00000368567.4:c.7-107G>T	ENSP00000357555.4:n.7-107G>T
ENST00000392558.4:c.7-107G>T	ENSP00000376341.4:n.7-107G>T
ENST00000477151.1:n.135G>T
ENST00000493224.5:n.246G>T
NM_001030.4:c.7-107G>T	NP_001021.1:n.7-107G>T
NM_001030.6:c.7-107G>T MANE Select	NP_001021.1:n.7-107G>T
NM_001349946.1:c.-117G>T	NP_001336875.1:n.-117G>T
NM_001349947.1:c.-117G>T	NP_001336876.1:n.-117G>T
NM_001349946.2:c.-117G>T	NP_001336875.1:n.-117G>T
NM_001349947.2:c.-117G>T	NP_001336876.1:n.-117G>T