Canonical Allele Identifier: CA389441101
Gene: SRP54 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35011547G>A , CM000676.2:g.35011547G>A GRCh38
NC_000014.8:g.35480753G>A , CM000676.1:g.35480753G>A GRCh37
NC_000014.7:g.34550504G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216774.11:c.524G>A MANE Select ENSP00000216774.6:p.Gly175Glu
ENST00000546080.6:c.347G>A ENSP00000440629.2:p.Gly116Glu
ENST00000553923.2:n.802G>A
ENST00000555746.6:c.524G>A ENSP00000451647.2:p.Gly175Glu
ENST00000677561.1:n.810G>A
ENST00000677621.1:n.802G>A
ENST00000677647.1:c.524G>A ENSP00000504673.1:p.Gly175Glu
ENST00000678274.1:c.*254G>A ENSP00000504600.1:n.*254G>A
ENST00000678477.1:c.524G>A ENSP00000504671.1:p.Gly175Glu
ENST00000678519.1:c.*262G>A ENSP00000504376.1:n.*262G>A
ENST00000678627.1:c.434G>A ENSP00000504550.1:p.Gly145Glu
ENST00000678836.1:c.524G>A ENSP00000504412.1:p.Gly175Glu
ENST00000678963.1:c.524G>A ENSP00000504518.1:p.Gly175Glu
ENST00000679045.1:n.802G>A
ENST00000216774.10:c.524G>A ENSP00000216774.6:p.Gly175Glu
ENST00000546080.5:c.377G>A ENSP00000440629.1:p.Gly126Glu
ENST00000555557.5:c.332G>A ENSP00000451775.1:p.Gly111Glu
ENST00000556380.3:c.*87G>A ENSP00000451313.1:n.*87G>A
ENST00000556994.5:c.524G>A ENSP00000451818.1:p.Gly175Glu
NM_001146282.1:c.377G>A NP_001139754.1:p.Gly126Glu
NM_003136.3:c.524G>A NP_003127.1:p.Gly175Glu
XM_005268024.1:c.524G>A XP_005268081.1:p.Gly175Glu
XM_011537106.1:c.524G>A XP_011535408.1:p.Gly175Glu
XM_011537107.1:c.212G>A XP_011535409.1:p.Gly71Glu
XM_005268024.3:c.524G>A XP_005268081.1:p.Gly175Glu
XM_017021615.2:c.212G>A XP_016877104.1:p.Gly71Glu
NM_003136.4:c.524G>A MANE Select NP_003127.1:p.Gly175Glu
NM_001146282.2:c.377G>A NP_001139754.1:p.Gly126Glu