Canonical Allele Identifier: CA2841259588

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726600dup , CM000671.2:g.91726600dup	GRCh38
NC_000009.11:g.94488882dup , CM000671.1:g.94488882dup	GRCh37
NC_000009.10:g.93528703dup	NCBI36
NG_008089.1:g.228563dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1327dup MANE Select	ENSP00000364860.3:p.Gln443ProfsTer16
ENST00000375708.3:c.1327dup	ENSP00000364860.3:p.Gln443ProfsTer16
ENST00000375715.5:c.907dup	ENSP00000364867.1:p.Gln303ProfsTer16
ENST00000550066.5:n.1795dup
NM_004560.3:c.1327dup	NP_004551.2:p.Gln443ProfsTer16
XM_005252008.3:c.907dup	XP_005252065.1:p.Gln303ProfsTer16
XM_005252009.3:c.124dup	XP_005252066.1:p.Gln42ProfsTer16
XM_006717121.2:c.907dup	XP_006717184.1:p.Gln303ProfsTer16
XM_011518721.1:c.907dup	XP_011517023.1:p.Gln303ProfsTer16
NM_001318204.1:c.1293dup	NP_001305133.1:p.Ser432GlnfsTer?
XM_005252008.4:c.907dup	XP_005252065.1:p.Gln303ProfsTer16
XM_006717121.3:c.907dup	XP_006717184.1:p.Gln303ProfsTer16
XM_017014762.1:c.1318dup	XP_016870251.1:p.Gln440ProfsTer16
XM_017014763.1:c.907dup	XP_016870252.1:p.Gln303ProfsTer16
XR_001746315.1:n.1536dup
NM_004560.4:c.1327dup MANE Select	NP_004551.2:p.Gln443ProfsTer16
NM_001318204.2:c.1293dup	NP_001305133.1:p.Ser432GlnfsTer?