Canonical Allele Identifier: CA195321055

Gene: ROR2

Linked Data

• dbSNP Id: rs1013003781
• gnomAD v2: 9-94485850-TGA-T
• gnomAD v3: 9-91723568-TGA-T
• gnomAD v4: 9-91723568-TGA-T
• MyVariant Identifiers: chr9:g.94485851_94485852del (hg19) ; chr9:g.91723569_91723570del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723569_91723570del , CM000671.2:g.91723569_91723570del	GRCh38
NC_000009.11:g.94485851_94485852del , CM000671.1:g.94485851_94485852del	GRCh37
NC_000009.10:g.93525672_93525673del	NCBI36
NG_008089.1:g.231593_231594del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.*92_*93del MANE Select	ENSP00000364860.3:n.*92_*93del
ENST00000375708.3:c.*92_*93del	ENSP00000364860.3:n.*92_*93del
ENST00000375715.5:c.1920+584_1920+585del	ENSP00000364867.1:n.1920+584_1920+585del
ENST00000550066.5:n.3392_3393del
NM_004560.3:c.*92_*93del	NP_004551.2:n.*92_*93del
XM_005252008.3:c.*92_*93del	XP_005252065.1:n.*92_*93del
XM_005252009.3:c.*92_*93del	XP_005252066.1:n.*92_*93del
XM_006717121.2:c.*92_*93del	XP_006717184.1:n.*92_*93del
XM_011518721.1:c.*92_*93del	XP_011517023.1:n.*92_*93del
XM_005252008.4:c.*92_*93del	XP_005252065.1:n.*92_*93del
XM_006717121.3:c.*92_*93del	XP_006717184.1:n.*92_*93del
XM_017014762.1:c.*92_*93del	XP_016870251.1:n.*92_*93del
XM_017014763.1:c.*92_*93del	XP_016870252.1:n.*92_*93del
NM_004560.4:c.*92_*93del MANE Select	NP_004551.2:n.*92_*93del