Canonical Allele Identifier: CA1863921169

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723571T= , CM000671.2:g.91723571T=	GRCh38
NC_000009.11:g.94485853T= , CM000671.1:g.94485853T=	GRCh37
NC_000009.10:g.93525674T=	NCBI36
NG_008089.1:g.231592A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.*91A= MANE Select	ENSP00000364860.3:n.*91A=
ENST00000375708.3:c.*91A=	ENSP00000364860.3:n.*91A=
ENST00000375715.5:c.1920+583A=	ENSP00000364867.1:n.1920+583A=
ENST00000550066.5:n.3391A=
NM_004560.3:c.*91A=	NP_004551.2:n.*91A=
XM_005252008.3:c.*91A=	XP_005252065.1:n.*91A=
XM_005252009.3:c.*91A=	XP_005252066.1:n.*91A=
XM_006717121.2:c.*91A=	XP_006717184.1:n.*91A=
XM_011518721.1:c.*91A=	XP_011517023.1:n.*91A=
XM_005252008.4:c.*91A=	XP_005252065.1:n.*91A=
XM_006717121.3:c.*91A=	XP_006717184.1:n.*91A=
XM_017014762.1:c.*91A=	XP_016870251.1:n.*91A=
XM_017014763.1:c.*91A=	XP_016870252.1:n.*91A=
NM_004560.4:c.*91A= MANE Select	NP_004551.2:n.*91A=