Canonical Allele Identifier: CA3168431239

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91802913G= , CM000671.2:g.91802913G=	GRCh38
NC_000009.11:g.94565195G= , CM000671.1:g.94565195G=	GRCh37
NC_000009.10:g.93605016G=	NCBI36
NG_008089.1:g.152250C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.98-27095C= MANE Select	NP_004551.2:n.98-27095C=
ENST00000375708.4:c.98-27095C= MANE Select	ENSP00000364860.3:n.98-27095C=
NM_001318204.1:c.98-27095C=	NP_001305133.1:n.98-27095C=
NM_001318204.2:c.98-27095C=	NP_001305133.1:n.98-27095C=
NM_004560.3:c.98-27095C=	NP_004551.2:n.98-27095C=
ENST00000375708.3:c.98-27095C=	ENSP00000364860.3:n.98-27095C=
ENST00000375715.5:c.-323-27095C=	ENSP00000364867.1:n.-323-27095C=
ENST00000495386.5:n.361-27095C=
ENST00000546883.1:n.300-27095C=
ENST00000550066.5:n.566-27095C=
XM_005252008.3:c.-323-27095C=	XP_005252065.1:n.-323-27095C=
XM_005252008.4:c.-323-27095C=	XP_005252065.1:n.-323-27095C=
XM_006717121.2:c.-324+14524C=	XP_006717184.1:n.-324+14524C=
XM_006717121.3:c.-324+14524C=	XP_006717184.1:n.-324+14524C=
XM_011518721.1:c.-323-27095C=	XP_011517023.1:n.-323-27095C=
XM_017014762.1:c.88+21646C=	XP_016870251.1:n.88+21646C=
XM_017014763.1:c.-323-27095C=	XP_016870252.1:n.-323-27095C=
XR_001746315.1:n.341-27095C=