Canonical Allele Identifier: CA16486020

Gene: SRP54

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35014676A>C , CM000676.2:g.35014676A>C	GRCh38
NC_000014.8:g.35483882A>C , CM000676.1:g.35483882A>C	GRCh37
NC_000014.7:g.34553633A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003136.4:c.887-68A>C MANE Select	NP_003127.1:n.887-68A>C
ENST00000216774.11:c.887-68A>C MANE Select	ENSP00000216774.6:n.887-68A>C
NM_001146282.1:c.740-68A>C	NP_001139754.1:n.740-68A>C
NM_001146282.2:c.740-68A>C	NP_001139754.1:n.740-68A>C
NM_003136.3:c.887-68A>C	NP_003127.1:n.887-68A>C
ENST00000216774.10:c.887-68A>C	ENSP00000216774.6:n.887-68A>C
ENST00000546080.5:c.740-68A>C	ENSP00000440629.1:n.740-68A>C
ENST00000546080.6:c.710-68A>C	ENSP00000440629.2:n.710-68A>C
ENST00000553923.2:n.1165-68A>C
ENST00000555557.5:c.695-68A>C	ENSP00000451775.1:n.695-68A>C
ENST00000555746.6:c.887-68A>C	ENSP00000451647.2:n.887-68A>C
ENST00000556994.5:c.887-68A>C	ENSP00000451818.1:n.887-68A>C
ENST00000677561.1:n.1173-68A>C
ENST00000677621.1:n.1165-68A>C
ENST00000677647.1:c.887-68A>C	ENSP00000504673.1:n.887-68A>C
ENST00000678274.1:c.*617-68A>C	ENSP00000504600.1:n.*617-68A>C
ENST00000678477.1:c.*45-68A>C	ENSP00000504671.1:n.*45-68A>C
ENST00000678519.1:c.*625-68A>C	ENSP00000504376.1:n.*625-68A>C
ENST00000678627.1:c.797-68A>C	ENSP00000504550.1:n.797-68A>C
ENST00000678836.1:c.887-68A>C	ENSP00000504412.1:n.887-68A>C
ENST00000678963.1:c.887-68A>C	ENSP00000504518.1:n.887-68A>C
XM_005268024.1:c.887-68A>C	XP_005268081.1:n.887-68A>C
XM_005268024.3:c.887-68A>C	XP_005268081.1:n.887-68A>C
XM_011537106.1:c.887-68A>C	XP_011535408.1:n.887-68A>C
XM_011537107.1:c.575-68A>C	XP_011535409.1:n.575-68A>C
XM_017021615.2:c.575-68A>C	XP_016877104.1:n.575-68A>C