Canonical Allele Identifier: CA1863921566

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723781C= , CM000671.2:g.91723781C=	GRCh38
NC_000009.11:g.94486063C= , CM000671.1:g.94486063C=	GRCh37
NC_000009.10:g.93525884C=	NCBI36
NG_008089.1:g.231382G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2713G= MANE Select	ENSP00000364860.3:p.Ala905=
ENST00000375708.3:c.2713G=	ENSP00000364860.3:p.Ala905=
ENST00000375715.5:c.1920+373G=	ENSP00000364867.1:n.1920+373G=
ENST00000550066.5:n.3181G=
NM_004560.3:c.2713G=	NP_004551.2:p.Ala905=
XM_005252008.3:c.2293G=	XP_005252065.1:p.Ala765=
XM_005252009.3:c.1510G=	XP_005252066.1:p.Ala504=
XM_006717121.2:c.2293G=	XP_006717184.1:p.Ala765=
XM_011518721.1:c.2293G=	XP_011517023.1:p.Ala765=
XM_005252008.4:c.2293G=	XP_005252065.1:p.Ala765=
XM_006717121.3:c.2293G=	XP_006717184.1:p.Ala765=
XM_017014762.1:c.2704G=	XP_016870251.1:p.Ala902=
XM_017014763.1:c.2293G=	XP_016870252.1:p.Ala765=
NM_004560.4:c.2713G= MANE Select	NP_004551.2:p.Ala905=