Canonical Allele Identifier: CA5120318

Gene: ROR2

Linked Data

• dbSNP Id: rs746756515
• ExAC: 9:94486025 TTCC / T
• gnomAD v2: 9-94486025-TTCC-T
• gnomAD v4: 9-91723743-TTCC-T
• COSMIC: COSM4722399
• MyVariant Identifiers: chr9:g.94486026_94486028del (hg19) ; chr9:g.91723744_91723746del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723755_91723757del , CM000671.2:g.91723755_91723757del	GRCh38
NC_000009.11:g.94486037_94486039del , CM000671.1:g.94486037_94486039del	GRCh37
NC_000009.10:g.93525858_93525860del	NCBI36
NG_008089.1:g.231417_231419del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2748_2750del MANE Select	ENSP00000364860.3:p.Glu917del
ENST00000375708.3:c.2748_2750del	ENSP00000364860.3:p.Glu917del
ENST00000375715.5:c.1920+408_1920+410del	ENSP00000364867.1:n.1920+408_1920+410del
ENST00000550066.5:n.3216_3218del
NM_004560.3:c.2748_2750del	NP_004551.2:p.Glu917del
XM_005252008.3:c.2328_2330del	XP_005252065.1:p.Glu777del
XM_005252009.3:c.1545_1547del	XP_005252066.1:p.Glu516del
XM_006717121.2:c.2328_2330del	XP_006717184.1:p.Glu777del
XM_011518721.1:c.2328_2330del	XP_011517023.1:p.Glu777del
XM_005252008.4:c.2328_2330del	XP_005252065.1:p.Glu777del
XM_006717121.3:c.2328_2330del	XP_006717184.1:p.Glu777del
XM_017014762.1:c.2739_2741del	XP_016870251.1:p.Glu914del
XM_017014763.1:c.2328_2330del	XP_016870252.1:p.Glu777del
NM_004560.4:c.2748_2750del MANE Select	NP_004551.2:p.Glu917del