Canonical Allele Identifier: CA589155667

Gene: ROR2

Linked Data

• dbSNP Id: rs1161670343
• gnomAD v2: 9-94485993-TC-T
• gnomAD v4: 9-91723711-TC-T
• MyVariant Identifiers: chr9:g.94485994del (hg19) ; chr9:g.91723712del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723716del , CM000671.2:g.91723716del	GRCh38
NC_000009.11:g.94485998del , CM000671.1:g.94485998del	GRCh37
NC_000009.10:g.93525819del	NCBI36
NG_008089.1:g.231451del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2782del MANE Select	ENSP00000364860.3:p.Asp928ThrfsTer?
ENST00000375708.3:c.2782del	ENSP00000364860.3:p.Asp928ThrfsTer?
ENST00000375715.5:c.1920+442del	ENSP00000364867.1:n.1920+442del
ENST00000550066.5:n.3250del
NM_004560.3:c.2782del	NP_004551.2:p.Asp928ThrfsTer?
XM_005252008.3:c.2362del	XP_005252065.1:p.Asp788ThrfsTer?
XM_005252009.3:c.1579del	XP_005252066.1:p.Asp527ThrfsTer?
XM_006717121.2:c.2362del	XP_006717184.1:p.Asp788ThrfsTer?
XM_011518721.1:c.2362del	XP_011517023.1:p.Asp788ThrfsTer?
XM_005252008.4:c.2362del	XP_005252065.1:p.Asp788ThrfsTer?
XM_006717121.3:c.2362del	XP_006717184.1:p.Asp788ThrfsTer?
XM_017014762.1:c.2773del	XP_016870251.1:p.Asp925ThrfsTer?
XM_017014763.1:c.2362del	XP_016870252.1:p.Asp788ThrfsTer?
NM_004560.4:c.2782del MANE Select	NP_004551.2:p.Asp928ThrfsTer?