Canonical Allele Identifier: CA2690635355

Gene: ROR2

Linked Data

• gnomAD v4: 9-91757515-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757517del , CM000671.2:g.91757517del	GRCh38
NC_000009.11:g.94519799del , CM000671.1:g.94519799del	GRCh37
NC_000009.10:g.93559620del	NCBI36
NG_008089.1:g.197647del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.219del MANE Select	ENSP00000364860.3:p.Ile73MetfsTer24
ENST00000375708.3:c.219del	ENSP00000364860.3:p.Ile73MetfsTer24
ENST00000375715.5:c.-202del	ENSP00000364867.1:n.-202del
ENST00000495386.5:n.482del
ENST00000546883.1:n.421del
ENST00000548585.2:n.85del
ENST00000550066.5:n.687del
NM_004560.3:c.219del	NP_004551.2:p.Ile73MetfsTer24
XM_005252008.3:c.-202del	XP_005252065.1:n.-202del
XM_006717121.2:c.-202del	XP_006717184.1:n.-202del
XM_011518721.1:c.-202del	XP_011517023.1:n.-202del
NM_001318204.1:c.219del	NP_001305133.1:p.Ile73MetfsTer24
XM_005252008.4:c.-202del	XP_005252065.1:n.-202del
XM_006717121.3:c.-202del	XP_006717184.1:n.-202del
XM_017014762.1:c.210del	XP_016870251.1:p.Ile70MetfsTer24
XM_017014763.1:c.-202del	XP_016870252.1:n.-202del
XR_001746315.1:n.462del
NM_004560.4:c.219del MANE Select	NP_004551.2:p.Ile73MetfsTer24
NM_001318204.2:c.219del	NP_001305133.1:p.Ile73MetfsTer24