Canonical Allele Identifier: CA2648113869

Gene: RPS27

Linked Data

• gnomAD v4: 1-153990886-GTCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990889_153990891del , CM000663.2:g.153990889_153990891del	GRCh38
NC_000001.10:g.153963365_153963367del , CM000663.1:g.153963365_153963367del	GRCh37
NC_000001.9:g.152229989_152229991del	NCBI36
NG_053102.2:g.5135_5137del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.7-25_7-23del	ENSP00000495765.1:n.7-25_7-23del
ENST00000651669.1:c.6+87_6+89del MANE Select	ENSP00000499044.1:n.6+87_6+89del
ENST00000368567.4:c.6+87_6+89del	ENSP00000357555.4:n.6+87_6+89del
ENST00000392558.4:c.6+87_6+89del	ENSP00000376341.4:n.6+87_6+89del
ENST00000477151.1:n.41-25_41-23del
ENST00000493224.5:n.127_129del
NM_001030.4:c.6+87_6+89del	NP_001021.1:n.6+87_6+89del
NM_001030.6:c.6+87_6+89del MANE Select	NP_001021.1:n.6+87_6+89del
NM_001349946.1:c.-211-25_-211-23del	NP_001336875.1:n.-211-25_-211-23del
NM_001349947.1:c.-236_-234del	NP_001336876.1:n.-236_-234del
NM_001349946.2:c.-211-25_-211-23del	NP_001336875.1:n.-211-25_-211-23del
NM_001349947.2:c.-236_-234del	NP_001336876.1:n.-236_-234del