Canonical Allele Identifier: CA1863925709

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726693T= , CM000671.2:g.91726693T=	GRCh38
NC_000009.11:g.94488975T= , CM000671.1:g.94488975T=	GRCh37
NC_000009.10:g.93528796T=	NCBI36
NG_008089.1:g.228470A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1234A= MANE Select	ENSP00000364860.3:p.Ile412=
ENST00000375708.3:c.1234A=	ENSP00000364860.3:p.Ile412=
ENST00000375715.5:c.814A=	ENSP00000364867.1:p.Ile272=
ENST00000550066.5:n.1702A=
NM_004560.3:c.1234A=	NP_004551.2:p.Ile412=
XM_005252008.3:c.814A=	XP_005252065.1:p.Ile272=
XM_005252009.3:c.31A=	XP_005252066.1:p.Ile11=
XM_006717121.2:c.814A=	XP_006717184.1:p.Ile272=
XM_011518721.1:c.814A=	XP_011517023.1:p.Ile272=
NM_001318204.1:c.1200A=	NP_001305133.1:p.Ala400=
XM_005252008.4:c.814A=	XP_005252065.1:p.Ile272=
XM_006717121.3:c.814A=	XP_006717184.1:p.Ile272=
XM_017014762.1:c.1225A=	XP_016870251.1:p.Ile409=
XM_017014763.1:c.814A=	XP_016870252.1:p.Ile272=
XR_001746315.1:n.1443A=
NM_004560.4:c.1234A= MANE Select	NP_004551.2:p.Ile412=
NM_001318204.2:c.1200A=	NP_001305133.1:p.Ala400=