Canonical Allele Identifier: CA5120321

Gene: ROR2

Linked Data

• dbSNP Id: rs770797925
• ExAC: 9:94486037 CTCT / C
• gnomAD v2: 9-94486037-CTCT-C
• gnomAD v3: 9-91723755-CTCT-C
• gnomAD v4: 9-91723755-CTCT-C
• MyVariant Identifiers: chr9:g.94486038_94486040del (hg19) ; chr9:g.91723756_91723758del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723756_91723758del , CM000671.2:g.91723756_91723758del	GRCh38
NC_000009.11:g.94486038_94486040del , CM000671.1:g.94486038_94486040del	GRCh37
NC_000009.10:g.93525859_93525861del	NCBI36
NG_008089.1:g.231405_231407del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2736_2738del MANE Select	ENSP00000364860.3:p.Glu913del
ENST00000375708.3:c.2736_2738del	ENSP00000364860.3:p.Glu913del
ENST00000375715.5:c.1920+396_1920+398del	ENSP00000364867.1:n.1920+396_1920+398del
ENST00000550066.5:n.3204_3206del
NM_004560.3:c.2736_2738del	NP_004551.2:p.Glu913del
XM_005252008.3:c.2316_2318del	XP_005252065.1:p.Glu773del
XM_005252009.3:c.1533_1535del	XP_005252066.1:p.Glu512del
XM_006717121.2:c.2316_2318del	XP_006717184.1:p.Glu773del
XM_011518721.1:c.2316_2318del	XP_011517023.1:p.Glu773del
XM_005252008.4:c.2316_2318del	XP_005252065.1:p.Glu773del
XM_006717121.3:c.2316_2318del	XP_006717184.1:p.Glu773del
XM_017014762.1:c.2727_2729del	XP_016870251.1:p.Glu910del
XM_017014763.1:c.2316_2318del	XP_016870252.1:p.Glu773del
NM_004560.4:c.2736_2738del MANE Select	NP_004551.2:p.Glu913del