Canonical Allele Identifier: CA1863921401

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723700G= , CM000671.2:g.91723700G=	GRCh38
NC_000009.11:g.94485982G= , CM000671.1:g.94485982G=	GRCh37
NC_000009.10:g.93525803G=	NCBI36
NG_008089.1:g.231463C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2794C= MANE Select	ENSP00000364860.3:p.Leu932=
ENST00000375708.3:c.2794C=	ENSP00000364860.3:p.Leu932=
ENST00000375715.5:c.1920+454C=	ENSP00000364867.1:n.1920+454C=
ENST00000550066.5:n.3262C=
NM_004560.3:c.2794C=	NP_004551.2:p.Leu932=
XM_005252008.3:c.2374C=	XP_005252065.1:p.Leu792=
XM_005252009.3:c.1591C=	XP_005252066.1:p.Leu531=
XM_006717121.2:c.2374C=	XP_006717184.1:p.Leu792=
XM_011518721.1:c.2374C=	XP_011517023.1:p.Leu792=
XM_005252008.4:c.2374C=	XP_005252065.1:p.Leu792=
XM_006717121.3:c.2374C=	XP_006717184.1:p.Leu792=
XM_017014762.1:c.2785C=	XP_016870251.1:p.Leu929=
XM_017014763.1:c.2374C=	XP_016870252.1:p.Leu792=
NM_004560.4:c.2794C= MANE Select	NP_004551.2:p.Leu932=