Canonical Allele Identifier: CA1863925406

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726538G= , CM000671.2:g.91726538G=	GRCh38
NC_000009.11:g.94488820G= , CM000671.1:g.94488820G=	GRCh37
NC_000009.10:g.93528641G=	NCBI36
NG_008089.1:g.228625C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1386+3C= MANE Select	ENSP00000364860.3:n.1386+3C=
ENST00000375708.3:c.1386+3C=	ENSP00000364860.3:n.1386+3C=
ENST00000375715.5:c.966+3C=	ENSP00000364867.1:n.966+3C=
ENST00000550066.5:n.1854+3C=
NM_004560.3:c.1386+3C=	NP_004551.2:n.1386+3C=
XM_005252008.3:c.966+3C=	XP_005252065.1:n.966+3C=
XM_005252009.3:c.183+3C=	XP_005252066.1:n.183+3C=
XM_006717121.2:c.966+3C=	XP_006717184.1:n.966+3C=
XM_011518721.1:c.966+3C=	XP_011517023.1:n.966+3C=
NM_001318204.1:c.*56C=	NP_001305133.1:n.*56C=
XM_005252008.4:c.966+3C=	XP_005252065.1:n.966+3C=
XM_006717121.3:c.966+3C=	XP_006717184.1:n.966+3C=
XM_017014762.1:c.1377+3C=	XP_016870251.1:n.1377+3C=
XM_017014763.1:c.966+3C=	XP_016870252.1:n.966+3C=
XR_001746315.1:n.1595+3C=
NM_004560.4:c.1386+3C= MANE Select	NP_004551.2:n.1386+3C=
NM_001318204.2:c.*56C=	NP_001305133.1:n.*56C=