Canonical Allele Identifier: CA2599989601

Gene: ROR2

Linked Data

• dbSNP Id: rs2118602504
• gnomAD v3: 9-91723549-A-ACTGGCCGG
• gnomAD v4: 9-91723549-A-ACTGGCCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723551_91723558dup , CM000671.2:g.91723551_91723558dup	GRCh38
NC_000009.11:g.94485833_94485840dup , CM000671.1:g.94485833_94485840dup	GRCh37
NC_000009.10:g.93525654_93525661dup	NCBI36
NG_008089.1:g.231606_231613dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.*105_*112dup MANE Select	ENSP00000364860.3:n.*105_*112dup
ENST00000375708.3:c.*105_*112dup	ENSP00000364860.3:n.*105_*112dup
ENST00000375715.5:c.1920+597_1920+604dup	ENSP00000364867.1:n.1920+597_1920+604dup
ENST00000550066.5:n.3405_3412dup
NM_004560.3:c.*105_*112dup	NP_004551.2:n.*105_*112dup
XM_005252008.3:c.*105_*112dup	XP_005252065.1:n.*105_*112dup
XM_005252009.3:c.*105_*112dup	XP_005252066.1:n.*105_*112dup
XM_006717121.2:c.*105_*112dup	XP_006717184.1:n.*105_*112dup
XM_011518721.1:c.*105_*112dup	XP_011517023.1:n.*105_*112dup
XM_005252008.4:c.*105_*112dup	XP_005252065.1:n.*105_*112dup
XM_006717121.3:c.*105_*112dup	XP_006717184.1:n.*105_*112dup
XM_017014762.1:c.*105_*112dup	XP_016870251.1:n.*105_*112dup
XM_017014763.1:c.*105_*112dup	XP_016870252.1:n.*105_*112dup
NM_004560.4:c.*105_*112dup MANE Select	NP_004551.2:n.*105_*112dup