Canonical Allele Identifier: CA5120802

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91731006C>T , CM000671.2:g.91731006C>T	GRCh38
NC_000009.11:g.94493288C>T , CM000671.1:g.94493288C>T	GRCh37
NC_000009.10:g.93533109C>T	NCBI36
NG_008089.1:g.224157G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.1087G>A MANE Select	NP_004551.2:p.Ala363Thr
ENST00000375708.4:c.1087G>A MANE Select	ENSP00000364860.3:p.Ala363Thr
NM_001318204.1:c.1087G>A	NP_001305133.1:p.Ala363Thr
NM_001318204.2:c.1087G>A	NP_001305133.1:p.Ala363Thr
NM_004560.3:c.1087G>A	NP_004551.2:p.Ala363Thr
ENST00000375708.3:c.1087G>A	ENSP00000364860.3:p.Ala363Thr
ENST00000375715.5:c.667G>A	ENSP00000364867.1:p.Ala223Thr
ENST00000550066.5:n.1555G>A
XM_005252008.3:c.667G>A	XP_005252065.1:p.Ala223Thr
XM_005252008.4:c.667G>A	XP_005252065.1:p.Ala223Thr
XM_005252009.3:c.-83G>A	XP_005252066.1:n.-83G>A
XM_006717121.2:c.667G>A	XP_006717184.1:p.Ala223Thr
XM_006717121.3:c.667G>A	XP_006717184.1:p.Ala223Thr
XM_011518721.1:c.667G>A	XP_011517023.1:p.Ala223Thr
XM_017014762.1:c.1078G>A	XP_016870251.1:p.Ala360Thr
XM_017014763.1:c.667G>A	XP_016870252.1:p.Ala223Thr
XR_001746315.1:n.1330G>A