Canonical Allele Identifier: CA2648114059

Gene: RPS27

Linked Data

• gnomAD v4: 1-153991067-CCATTTTCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991069_153991076del , CM000663.2:g.153991069_153991076del	GRCh38
NC_000001.10:g.153963545_153963552del , CM000663.1:g.153963545_153963552del	GRCh37
NC_000001.9:g.152230169_152230176del	NCBI36
NG_053102.2:g.5315_5322del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.149_156del
ENST00000643794.1:c.127+35_128-39del	ENSP00000495765.1:n.127+35_128-39del
ENST00000651669.1:c.7-46_7-39del MANE Select	ENSP00000499044.1:n.7-46_7-39del
ENST00000368567.4:c.7-46_7-39del	ENSP00000357555.4:n.7-46_7-39del
ENST00000392558.4:c.7-46_7-39del	ENSP00000376341.4:n.7-46_7-39del
ENST00000477151.1:n.161+35_162-39del
ENST00000493224.5:n.272+35_273-39del
NM_001030.4:c.7-46_7-39del	NP_001021.1:n.7-46_7-39del
NM_001030.6:c.7-46_7-39del MANE Select	NP_001021.1:n.7-46_7-39del
NM_001349946.1:c.-91+35_-90-39del	NP_001336875.1:n.-91+35_-90-39del
NM_001349947.1:c.-91+35_-90-39del	NP_001336876.1:n.-91+35_-90-39del
NM_001349946.2:c.-91+35_-90-39del	NP_001336875.1:n.-91+35_-90-39del
NM_001349947.2:c.-91+35_-90-39del	NP_001336876.1:n.-91+35_-90-39del