Canonical Allele Identifier: CA5120583

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724748C>T , CM000671.2:g.91724748C>T	GRCh38
NC_000009.11:g.94487030C>T , CM000671.1:g.94487030C>T	GRCh37
NC_000009.10:g.93526851C>T	NCBI36
NG_008089.1:g.230415G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.1746G>A MANE Select	NP_004551.2:p.Thr582=
ENST00000375708.4:c.1746G>A MANE Select	ENSP00000364860.3:p.Thr582=
NM_004560.3:c.1746G>A	NP_004551.2:p.Thr582=
ENST00000375708.3:c.1746G>A	ENSP00000364860.3:p.Thr582=
ENST00000375715.5:c.1326G>A	ENSP00000364867.1:p.Thr442=
ENST00000550066.5:n.2214G>A
XM_005252008.3:c.1326G>A	XP_005252065.1:p.Thr442=
XM_005252008.4:c.1326G>A	XP_005252065.1:p.Thr442=
XM_005252009.3:c.543G>A	XP_005252066.1:p.Thr181=
XM_006717121.2:c.1326G>A	XP_006717184.1:p.Thr442=
XM_006717121.3:c.1326G>A	XP_006717184.1:p.Thr442=
XM_011518721.1:c.1326G>A	XP_011517023.1:p.Thr442=
XM_017014762.1:c.1737G>A	XP_016870251.1:p.Thr579=
XM_017014763.1:c.1326G>A	XP_016870252.1:p.Thr442=