Canonical Allele Identifier: CA2839057624

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723858del , CM000671.2:g.91723858del	GRCh38
NC_000009.11:g.94486140del , CM000671.1:g.94486140del	GRCh37
NC_000009.10:g.93525961del	NCBI36
NG_008089.1:g.231306del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2637del MANE Select	ENSP00000364860.3:p.Asn880ThrfsTer?
ENST00000375708.3:c.2637del	ENSP00000364860.3:p.Asn880ThrfsTer?
ENST00000375715.5:c.1920+297del	ENSP00000364867.1:n.1920+297del
ENST00000550066.5:n.3105del
NM_004560.3:c.2637del	NP_004551.2:p.Asn880ThrfsTer?
XM_005252008.3:c.2217del	XP_005252065.1:p.Asn740ThrfsTer?
XM_005252009.3:c.1434del	XP_005252066.1:p.Asn479ThrfsTer?
XM_006717121.2:c.2217del	XP_006717184.1:p.Asn740ThrfsTer?
XM_011518721.1:c.2217del	XP_011517023.1:p.Asn740ThrfsTer?
XM_005252008.4:c.2217del	XP_005252065.1:p.Asn740ThrfsTer?
XM_006717121.3:c.2217del	XP_006717184.1:p.Asn740ThrfsTer?
XM_017014762.1:c.2628del	XP_016870251.1:p.Asn877ThrfsTer?
XM_017014763.1:c.2217del	XP_016870252.1:p.Asn740ThrfsTer?
NM_004560.4:c.2637del MANE Select	NP_004551.2:p.Asn880ThrfsTer?