Canonical Allele Identifier: CA2480680237

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990813_153990820delinsTGGTCCAG , CM000663.2:g.153990813_153990820delinsTGGTCCAG	GRCh38
NC_000001.10:g.153963289_153963296delinsTGGTCCAG , CM000663.1:g.153963289_153963296delinsTGGTCCAG	GRCh37
NC_000001.9:g.152229913_152229920delinsTGGTCCAG	NCBI36
NG_053102.2:g.5059_5066delinsTGGTCCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.6+11_6+18delinsTGGTCCAG	ENSP00000495765.1:n.6+11_6+18delinsTGGTCCAG
ENST00000651669.1:c.6+11_6+18delinsTGGTCCAG MANE Select	ENSP00000499044.1:n.6+11_6+18delinsTGGTCCAG
ENST00000368567.4:c.6+11_6+18delinsTGGTCCAG	ENSP00000357555.4:n.6+11_6+18delinsTGGTCCAG
ENST00000392558.4:c.6+11_6+18delinsTGGTCCAG	ENSP00000376341.4:n.6+11_6+18delinsTGGTCCAG
ENST00000477151.1:n.40+11_40+18delinsTGGTCCAG
ENST00000493224.5:n.51_58delinsTGGTCCAG
NM_001030.4:c.6+11_6+18delinsTGGTCCAG	NP_001021.1:n.6+11_6+18delinsTGGTCCAG
NM_001030.6:c.6+11_6+18delinsTGGTCCAG MANE Select	NP_001021.1:n.6+11_6+18delinsTGGTCCAG
NM_001349946.1:c.-212+11_-212+18delinsTGGTCCAG	NP_001336875.1:n.-212+11_-212+18delinsTGGTCCAG
NM_001349947.1:c.-312_-305delinsTGGTCCAG	NP_001336876.1:n.-312_-305delinsTGGTCCAG
NM_001349946.2:c.-212+11_-212+18delinsTGGTCCAG	NP_001336875.1:n.-212+11_-212+18delinsTGGTCCAG
NM_001349947.2:c.-312_-305delinsTGGTCCAG	NP_001336876.1:n.-312_-305delinsTGGTCCAG