Canonical Allele Identifier: CA653173399

Gene: ROR2

Linked Data

• COSMIC: COSN23017498

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723556_91723557insA , CM000671.2:g.91723556_91723557insA	GRCh38
NC_000009.11:g.94485838_94485839insA , CM000671.1:g.94485838_94485839insA	GRCh37
NC_000009.10:g.93525659_93525660insA	NCBI36
NG_008089.1:g.231606_231607insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.*105_*106insT MANE Select	ENSP00000364860.3:n.*105_*106insT
ENST00000375708.3:c.*105_*106insT	ENSP00000364860.3:n.*105_*106insT
ENST00000375715.5:c.1920+597_1920+598insT	ENSP00000364867.1:n.1920+597_1920+598insT
ENST00000550066.5:n.3405_3406insT
NM_004560.3:c.*105_*106insT	NP_004551.2:n.*105_*106insT
XM_005252008.3:c.*105_*106insT	XP_005252065.1:n.*105_*106insT
XM_005252009.3:c.*105_*106insT	XP_005252066.1:n.*105_*106insT
XM_006717121.2:c.*105_*106insT	XP_006717184.1:n.*105_*106insT
XM_011518721.1:c.*105_*106insT	XP_011517023.1:n.*105_*106insT
XM_005252008.4:c.*105_*106insT	XP_005252065.1:n.*105_*106insT
XM_006717121.3:c.*105_*106insT	XP_006717184.1:n.*105_*106insT
XM_017014762.1:c.*105_*106insT	XP_016870251.1:n.*105_*106insT
XM_017014763.1:c.*105_*106insT	XP_016870252.1:n.*105_*106insT
NM_004560.4:c.*105_*106insT MANE Select	NP_004551.2:n.*105_*106insT