Canonical Allele Identifier: CA465996871
Gene: ROR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91726694G>A , CM000671.2:g.91726694G>A GRCh38
NC_000009.11:g.94488976G>A , CM000671.1:g.94488976G>A GRCh37
NC_000009.10:g.93528797G>A NCBI36
NG_008089.1:g.228469C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.1233C>T MANE Select ENSP00000364860.3:p.Ser411=
ENST00000375708.3:c.1233C>T ENSP00000364860.3:p.Ser411=
ENST00000375715.5:c.813C>T ENSP00000364867.1:p.Ser271=
ENST00000550066.5:n.1701C>T
NM_004560.3:c.1233C>T NP_004551.2:p.Ser411=
XM_005252008.3:c.813C>T XP_005252065.1:p.Ser271=
XM_005252009.3:c.30C>T XP_005252066.1:p.Ser10=
XM_006717121.2:c.813C>T XP_006717184.1:p.Ser271=
XM_011518721.1:c.813C>T XP_011517023.1:p.Ser271=
NM_001318204.1:c.1199C>T NP_001305133.1:p.Ala400Val
XM_005252008.4:c.813C>T XP_005252065.1:p.Ser271=
XM_006717121.3:c.813C>T XP_006717184.1:p.Ser271=
XM_017014762.1:c.1224C>T XP_016870251.1:p.Ser408=
XM_017014763.1:c.813C>T XP_016870252.1:p.Ser271=
XR_001746315.1:n.1442C>T
NM_004560.4:c.1233C>T MANE Select NP_004551.2:p.Ser411=
NM_001318204.2:c.1199C>T NP_001305133.1:p.Ala400Val