Canonical Allele Identifier: CA1863923361

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757522G= , CM000671.2:g.91757522G=	GRCh38
NC_000009.11:g.94519804G= , CM000671.1:g.94519804G=	GRCh37
NC_000009.10:g.93559625G=	NCBI36
NG_008089.1:g.197641C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.213C= MANE Select	ENSP00000364860.3:p.Ile71=
ENST00000375708.3:c.213C=	ENSP00000364860.3:p.Ile71=
ENST00000375715.5:c.-208C=	ENSP00000364867.1:n.-208C=
ENST00000495386.5:n.476C=
ENST00000546883.1:n.415C=
ENST00000548585.2:n.79C=
ENST00000550066.5:n.681C=
NM_004560.3:c.213C=	NP_004551.2:p.Ile71=
XM_005252008.3:c.-208C=	XP_005252065.1:n.-208C=
XM_006717121.2:c.-208C=	XP_006717184.1:n.-208C=
XM_011518721.1:c.-208C=	XP_011517023.1:n.-208C=
NM_001318204.1:c.213C=	NP_001305133.1:p.Ile71=
XM_005252008.4:c.-208C=	XP_005252065.1:n.-208C=
XM_006717121.3:c.-208C=	XP_006717184.1:n.-208C=
XM_017014762.1:c.204C=	XP_016870251.1:p.Ile68=
XM_017014763.1:c.-208C=	XP_016870252.1:n.-208C=
XR_001746315.1:n.456C=
NM_004560.4:c.213C= MANE Select	NP_004551.2:p.Ile71=
NM_001318204.2:c.213C=	NP_001305133.1:p.Ile71=