Canonical Allele Identifier: CA2690632113

Gene: ROR2

Linked Data

• gnomAD v4: 9-91723477-GGCAGGGCAGCTCTCTGTGTCAGAGGACAGAGAGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723485_91723519del , CM000671.2:g.91723485_91723519del	GRCh38
NC_000009.11:g.94485767_94485801del , CM000671.1:g.94485767_94485801del	GRCh37
NC_000009.10:g.93525588_93525622del	NCBI36
NG_008089.1:g.231651_231685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.*150_*184del MANE Select	ENSP00000364860.3:n.*150_*184del
ENST00000375708.3:c.*150_*184del	ENSP00000364860.3:n.*150_*184del
ENST00000375715.5:c.1920+642_1920+676del	ENSP00000364867.1:n.1920+642_1920+676del
ENST00000550066.5:n.3450_3484del
NM_004560.3:c.*150_*184del	NP_004551.2:n.*150_*184del
XM_005252008.3:c.*150_*184del	XP_005252065.1:n.*150_*184del
XM_005252009.3:c.*150_*184del	XP_005252066.1:n.*150_*184del
XM_006717121.2:c.*150_*184del	XP_006717184.1:n.*150_*184del
XM_011518721.1:c.*150_*184del	XP_011517023.1:n.*150_*184del
XM_005252008.4:c.*150_*184del	XP_005252065.1:n.*150_*184del
XM_006717121.3:c.*150_*184del	XP_006717184.1:n.*150_*184del
XM_017014762.1:c.*150_*184del	XP_016870251.1:n.*150_*184del
XM_017014763.1:c.*150_*184del	XP_016870252.1:n.*150_*184del
NM_004560.4:c.*150_*184del MANE Select	NP_004551.2:n.*150_*184del