Canonical Allele Identifier: CA485881949

Gene: SRP54

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35007378A>G , CM000676.2:g.35007378A>G	GRCh38
NC_000014.8:g.35476584A>G , CM000676.1:g.35476584A>G	GRCh37
NC_000014.7:g.34546335A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216774.11:c.351A>G MANE Select	ENSP00000216774.6:p.Thr117=
ENST00000546080.6:c.174A>G	ENSP00000440629.2:p.Thr58=
ENST00000553923.2:n.629A>G
ENST00000555746.6:c.351A>G	ENSP00000451647.2:p.Thr117=
ENST00000677561.1:n.637A>G
ENST00000677621.1:n.629A>G
ENST00000677647.1:c.351A>G	ENSP00000504673.1:p.Thr117=
ENST00000678274.1:c.*89A>G	ENSP00000504600.1:n.*89A>G
ENST00000678477.1:c.351A>G	ENSP00000504671.1:p.Thr117=
ENST00000678519.1:c.*89A>G	ENSP00000504376.1:n.*89A>G
ENST00000678627.1:c.261A>G	ENSP00000504550.1:p.Thr87=
ENST00000678836.1:c.351A>G	ENSP00000504412.1:p.Thr117=
ENST00000678963.1:c.351A>G	ENSP00000504518.1:p.Thr117=
ENST00000679045.1:n.629A>G
ENST00000216774.10:c.351A>G	ENSP00000216774.6:p.Thr117=
ENST00000546080.5:c.204A>G	ENSP00000440629.1:p.Thr68=
ENST00000555557.5:c.159A>G	ENSP00000451775.1:p.Thr53=
ENST00000556380.3:c.117-1274A>G	ENSP00000451313.1:n.117-1274A>G
ENST00000556994.5:c.351A>G	ENSP00000451818.1:p.Thr117=
ENST00000630962.1:c.117-1274A>G	ENSP00000486764.1:n.117-1274A>G
NM_001146282.1:c.204A>G	NP_001139754.1:p.Thr68=
NM_003136.3:c.351A>G	NP_003127.1:p.Thr117=
XM_005268024.1:c.351A>G	XP_005268081.1:p.Thr117=
XM_011537106.1:c.351A>G	XP_011535408.1:p.Thr117=
XM_011537107.1:c.39A>G	XP_011535409.1:p.Thr13=
XM_005268024.3:c.351A>G	XP_005268081.1:p.Thr117=
XM_017021615.2:c.39A>G	XP_016877104.1:p.Thr13=
NM_003136.4:c.351A>G MANE Select	NP_003127.1:p.Thr117=
NM_001146282.2:c.204A>G	NP_001139754.1:p.Thr68=