Canonical Allele Identifier: CA2690632375
Gene: ROR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91724539_91724553del , CM000671.2:g.91724539_91724553del GRCh38
NC_000009.11:g.94486821_94486835del , CM000671.1:g.94486821_94486835del GRCh37
NC_000009.10:g.93526642_93526656del NCBI36
NG_008089.1:g.230617_230631del

Transcript Alleles

HGVS Amino-acid change
ENST00000375708.4:c.1948_1962del MANE Select ENSP00000364860.3:p.Gly650_Leu654del
ENST00000375708.3:c.1948_1962del ENSP00000364860.3:p.Gly650_Leu654del
ENST00000375715.5:c.1528_1542del ENSP00000364867.1:p.Gly510_Leu514del
ENST00000550066.5:n.2416_2430del
NM_004560.3:c.1948_1962del NP_004551.2:p.Gly650_Leu654del
XM_005252008.3:c.1528_1542del XP_005252065.1:p.Gly510_Leu514del
XM_005252009.3:c.745_759del XP_005252066.1:p.Gly249_Leu253del
XM_006717121.2:c.1528_1542del XP_006717184.1:p.Gly510_Leu514del
XM_011518721.1:c.1528_1542del XP_011517023.1:p.Gly510_Leu514del
XM_005252008.4:c.1528_1542del XP_005252065.1:p.Gly510_Leu514del
XM_006717121.3:c.1528_1542del XP_006717184.1:p.Gly510_Leu514del
XM_017014762.1:c.1939_1953del XP_016870251.1:p.Gly647_Leu651del
XM_017014763.1:c.1528_1542del XP_016870252.1:p.Gly510_Leu514del
NM_004560.4:c.1948_1962del MANE Select NP_004551.2:p.Gly650_Leu654del