Canonical Allele Identifier: CA5120907
Gene: ROR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91733328C>T , CM000671.2:g.91733328C>T GRCh38
NC_000009.11:g.94495610C>T , CM000671.1:g.94495610C>T GRCh37
NC_000009.10:g.93535431C>T NCBI36
NG_008089.1:g.221835G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.731G>A MANE Select ENSP00000364860.3:p.Arg244Gln
ENST00000375708.3:c.731G>A ENSP00000364860.3:p.Arg244Gln
ENST00000375715.5:c.311G>A ENSP00000364867.1:p.Arg104Gln
ENST00000550066.5:n.1199G>A
NM_004560.3:c.731G>A NP_004551.2:p.Arg244Gln
XM_005252008.3:c.311G>A XP_005252065.1:p.Arg104Gln
XM_006717121.2:c.311G>A XP_006717184.1:p.Arg104Gln
XM_011518721.1:c.311G>A XP_011517023.1:p.Arg104Gln
NM_001318204.1:c.731G>A NP_001305133.1:p.Arg244Gln
XM_005252008.4:c.311G>A XP_005252065.1:p.Arg104Gln
XM_006717121.3:c.311G>A XP_006717184.1:p.Arg104Gln
XM_017014762.1:c.722G>A XP_016870251.1:p.Arg241Gln
XM_017014763.1:c.311G>A XP_016870252.1:p.Arg104Gln
XR_001746315.1:n.974G>A
NM_004560.4:c.731G>A MANE Select NP_004551.2:p.Arg244Gln
NM_001318204.2:c.731G>A NP_001305133.1:p.Arg244Gln