Canonical Allele Identifier: CA1863923321

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757463G= , CM000671.2:g.91757463G=	GRCh38
NC_000009.11:g.94519745G= , CM000671.1:g.94519745G=	GRCh37
NC_000009.10:g.93559566G=	NCBI36
NG_008089.1:g.197700C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.272C= MANE Select	ENSP00000364860.3:p.Pro91=
ENST00000375708.3:c.272C=	ENSP00000364860.3:p.Pro91=
ENST00000375715.5:c.-149C=	ENSP00000364867.1:n.-149C=
ENST00000495386.5:n.535C=
ENST00000546883.1:n.474C=
ENST00000548585.2:n.138C=
ENST00000550066.5:n.740C=
NM_004560.3:c.272C=	NP_004551.2:p.Pro91=
XM_005252008.3:c.-149C=	XP_005252065.1:n.-149C=
XM_006717121.2:c.-149C=	XP_006717184.1:n.-149C=
XM_011518721.1:c.-149C=	XP_011517023.1:n.-149C=
NM_001318204.1:c.272C=	NP_001305133.1:p.Pro91=
XM_005252008.4:c.-149C=	XP_005252065.1:n.-149C=
XM_006717121.3:c.-149C=	XP_006717184.1:n.-149C=
XM_017014762.1:c.263C=	XP_016870251.1:p.Pro88=
XM_017014763.1:c.-149C=	XP_016870252.1:n.-149C=
XR_001746315.1:n.515C=
NM_004560.4:c.272C= MANE Select	NP_004551.2:p.Pro91=
NM_001318204.2:c.272C=	NP_001305133.1:p.Pro91=