Canonical Allele Identifier: CA2648113847

Gene: RPS27

Linked Data

• gnomAD v4: 1-153990826-GGCGGAGATCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990829_153990839del , CM000663.2:g.153990829_153990839del	GRCh38
NC_000001.10:g.153963305_153963315del , CM000663.1:g.153963305_153963315del	GRCh37
NC_000001.9:g.152229929_152229939del	NCBI36
NG_053102.2:g.5075_5085del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.6+27_6+37del	ENSP00000495765.1:n.6+27_6+37del
ENST00000651669.1:c.6+27_6+37del MANE Select	ENSP00000499044.1:n.6+27_6+37del
ENST00000368567.4:c.6+27_6+37del	ENSP00000357555.4:n.6+27_6+37del
ENST00000392558.4:c.6+27_6+37del	ENSP00000376341.4:n.6+27_6+37del
ENST00000477151.1:n.40+27_40+37del
ENST00000493224.5:n.67_77del
NM_001030.4:c.6+27_6+37del	NP_001021.1:n.6+27_6+37del
NM_001030.6:c.6+27_6+37del MANE Select	NP_001021.1:n.6+27_6+37del
NM_001349946.1:c.-212+27_-212+37del	NP_001336875.1:n.-212+27_-212+37del
NM_001349947.1:c.-296_-286del	NP_001336876.1:n.-296_-286del
NM_001349946.2:c.-212+27_-212+37del	NP_001336875.1:n.-212+27_-212+37del
NM_001349947.2:c.-296_-286del	NP_001336876.1:n.-296_-286del