Canonical Allele Identifier: CA2480680343
Gene: RPS27 HGNC NCBI

Linked Data

dbSNP Id: rs1649363595

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990979_153990983dup , CM000663.2:g.153990979_153990983dup GRCh38
NC_000001.10:g.153963455_153963459dup , CM000663.1:g.153963455_153963459dup GRCh37
NC_000001.9:g.152230079_152230083dup NCBI36
NG_053102.2:g.5225_5229dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000477151.2:n.59_63dup
ENST00000643794.1:c.72_76dup ENSP00000495765.1:p.Trp26Ter
ENST00000651669.1:c.7-136_7-132dup MANE Select ENSP00000499044.1:n.7-136_7-132dup
ENST00000368567.4:c.7-136_7-132dup ENSP00000357555.4:n.7-136_7-132dup
ENST00000392558.4:c.7-136_7-132dup ENSP00000376341.4:n.7-136_7-132dup
ENST00000477151.1:n.106_110dup
ENST00000493224.5:n.217_221dup
NM_001030.4:c.7-136_7-132dup NP_001021.1:n.7-136_7-132dup
NM_001030.6:c.7-136_7-132dup MANE Select NP_001021.1:n.7-136_7-132dup
NM_001349946.1:c.-146_-142dup NP_001336875.1:n.-146_-142dup
NM_001349947.1:c.-146_-142dup NP_001336876.1:n.-146_-142dup
NM_001349946.2:c.-146_-142dup NP_001336875.1:n.-146_-142dup
NM_001349947.2:c.-146_-142dup NP_001336876.1:n.-146_-142dup