Canonical Allele Identifier: CA1863925506

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726593A= , CM000671.2:g.91726593A=	GRCh38
NC_000009.11:g.94488875A= , CM000671.1:g.94488875A=	GRCh37
NC_000009.10:g.93528696A=	NCBI36
NG_008089.1:g.228570T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1334T= MANE Select	ENSP00000364860.3:p.Met445=
ENST00000375708.3:c.1334T=	ENSP00000364860.3:p.Met445=
ENST00000375715.5:c.914T=	ENSP00000364867.1:p.Met305=
ENST00000550066.5:n.1802T=
NM_004560.3:c.1334T=	NP_004551.2:p.Met445=
XM_005252008.3:c.914T=	XP_005252065.1:p.Met305=
XM_005252009.3:c.131T=	XP_005252066.1:p.Met44=
XM_006717121.2:c.914T=	XP_006717184.1:p.Met305=
XM_011518721.1:c.914T=	XP_011517023.1:p.Met305=
NM_001318204.1:c.*1T=	NP_001305133.1:n.*1T=
XM_005252008.4:c.914T=	XP_005252065.1:p.Met305=
XM_006717121.3:c.914T=	XP_006717184.1:p.Met305=
XM_017014762.1:c.1325T=	XP_016870251.1:p.Met442=
XM_017014763.1:c.914T=	XP_016870252.1:p.Met305=
XR_001746315.1:n.1543T=
NM_004560.4:c.1334T= MANE Select	NP_004551.2:p.Met445=
NM_001318204.2:c.*1T=	NP_001305133.1:n.*1T=