Canonical Allele Identifier: CA2345185952

Gene: RBCK1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.419345A= , CM000682.2:g.419345A=	GRCh38
NC_000020.10:g.399989A= , CM000682.1:g.399989A=	GRCh37
NC_000020.9:g.347989A=	NCBI36
NG_033233.1:g.16281A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697804.1:c.461-2A=	ENSP00000513444.1:n.461-2A=
ENST00000697805.1:c.512-2A=	ENSP00000513446.1:n.512-2A=
ENST00000356286.10:c.461-2A= MANE Select	ENSP00000348632.6:n.461-2A=
ENST00000640614.1:c.112-2A=	ENSP00000491402.1:n.112-2A=
ENST00000353660.7:c.335-2A=	ENSP00000254960.5:n.335-2A=
ENST00000356286.9:c.461-2A=	ENSP00000348632.5:n.461-2A=
ENST00000382181.2:c.112-2A=	ENSP00000371616.2:n.112-2A=
ENST00000382214.7:c.461-2A=	ENSP00000371649.3:n.461-2A=
ENST00000414880.1:c.559-2A=
ENST00000415942.5:c.461-2A=	ENSP00000405288.1:n.461-2A=
NM_006462.4:c.335-2A=	NP_006453.1:n.335-2A=
NM_031229.2:c.461-2A=	NP_112506.2:n.461-2A=
XM_005260645.1:c.512-2A=	XP_005260702.1:n.512-2A=
XM_011529137.1:c.635-2A=	XP_011527439.1:n.635-2A=
XM_011529138.1:c.584-2A=	XP_011527440.1:n.584-2A=
XM_011529139.1:c.635-2A=	XP_011527441.1:n.635-2A=
XM_011529140.1:c.635-2A=	XP_011527442.1:n.635-2A=
XR_430267.1:n.920-2A=
XR_937029.1:n.1088-2A=
NM_001323956.1:c.112-2A=	NP_001310885.1:n.112-2A=
NM_001323958.1:c.112-2A=	NP_001310887.1:n.112-2A=
NM_006462.5:c.335-2A=	NP_006453.1:n.335-2A=
NM_031229.3:c.461-2A=	NP_112506.2:n.461-2A=
NR_136659.1:n.1169-2A=
XM_005260645.2:c.512-2A=	XP_005260702.1:n.512-2A=
XM_011529137.2:c.635-2A=	XP_011527439.1:n.635-2A=
XM_011529139.3:c.635-2A=	XP_011527441.1:n.635-2A=
XM_011529140.2:c.635-2A=	XP_011527442.1:n.635-2A=
XM_017027594.2:c.112-2A=	XP_016883083.1:n.112-2A=
XM_017027595.1:c.112-2A=	XP_016883084.1:n.112-2A=
XR_001754130.2:n.1094-2A=
XR_001754131.1:n.920-2A=
XR_937029.3:n.1094-2A=
NM_001323958.2:c.112-2A=	NP_001310887.1:n.112-2A=
NM_006462.6:c.335-2A=	NP_006453.1:n.335-2A=
NM_031229.4:c.461-2A= MANE Select	NP_112506.2:n.461-2A=
NR_136659.2:n.920-2A=
NM_001323956.2:c.112-2A=	NP_001310885.1:n.112-2A=