Canonical Allele Identifier: CA2690633361
Gene: ROR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91726696dup , CM000671.2:g.91726696dup GRCh38
NC_000009.11:g.94488978dup , CM000671.1:g.94488978dup GRCh37
NC_000009.10:g.93528799dup NCBI36
NG_008089.1:g.228467dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.1231dup MANE Select ENSP00000364860.3:p.Ser411LysfsTer21
ENST00000375708.3:c.1231dup ENSP00000364860.3:p.Ser411LysfsTer21
ENST00000375715.5:c.811dup ENSP00000364867.1:p.Ser271LysfsTer21
ENST00000550066.5:n.1699dup
NM_004560.3:c.1231dup NP_004551.2:p.Ser411LysfsTer21
XM_005252008.3:c.811dup XP_005252065.1:p.Ser271LysfsTer21
XM_005252009.3:c.28dup XP_005252066.1:p.Ser10LysfsTer21
XM_006717121.2:c.811dup XP_006717184.1:p.Ser271LysfsTer21
XM_011518721.1:c.811dup XP_011517023.1:p.Ser271LysfsTer21
NM_001318204.1:c.1197dup NP_001305133.1:p.Ala400SerfsTer?
XM_005252008.4:c.811dup XP_005252065.1:p.Ser271LysfsTer21
XM_006717121.3:c.811dup XP_006717184.1:p.Ser271LysfsTer21
XM_017014762.1:c.1222dup XP_016870251.1:p.Ser408LysfsTer21
XM_017014763.1:c.811dup XP_016870252.1:p.Ser271LysfsTer21
XR_001746315.1:n.1440dup
NM_004560.4:c.1231dup MANE Select NP_004551.2:p.Ser411LysfsTer21
NM_001318204.2:c.1197dup NP_001305133.1:p.Ala400SerfsTer?