Canonical Allele Identifier: CA2579378073
Gene: ROR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91757642_91757644dup , CM000671.2:g.91757642_91757644dup GRCh38
NC_000009.11:g.94519924_94519926dup , CM000671.1:g.94519924_94519926dup GRCh37
NC_000009.10:g.93559745_93559747dup NCBI36
NG_008089.1:g.197521_197523dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.176-83_176-81dup MANE Select ENSP00000364860.3:n.176-83_176-81dup
ENST00000375708.3:c.176-83_176-81dup ENSP00000364860.3:n.176-83_176-81dup
ENST00000375715.5:c.-245-83_-245-81dup ENSP00000364867.1:n.-245-83_-245-81dup
ENST00000495386.5:n.439-83_439-81dup
ENST00000546883.1:n.378-83_378-81dup
ENST00000548585.2:n.42-83_42-81dup
ENST00000550066.5:n.644-83_644-81dup
NM_004560.3:c.176-83_176-81dup NP_004551.2:n.176-83_176-81dup
XM_005252008.3:c.-245-83_-245-81dup XP_005252065.1:n.-245-83_-245-81dup
XM_006717121.2:c.-245-83_-245-81dup XP_006717184.1:n.-245-83_-245-81dup
XM_011518721.1:c.-245-83_-245-81dup XP_011517023.1:n.-245-83_-245-81dup
NM_001318204.1:c.176-83_176-81dup NP_001305133.1:n.176-83_176-81dup
XM_005252008.4:c.-245-83_-245-81dup XP_005252065.1:n.-245-83_-245-81dup
XM_006717121.3:c.-245-83_-245-81dup XP_006717184.1:n.-245-83_-245-81dup
XM_017014762.1:c.167-83_167-81dup XP_016870251.1:n.167-83_167-81dup
XM_017014763.1:c.-245-83_-245-81dup XP_016870252.1:n.-245-83_-245-81dup
XR_001746315.1:n.419-83_419-81dup
NM_004560.4:c.176-83_176-81dup MANE Select NP_004551.2:n.176-83_176-81dup
NM_001318204.2:c.176-83_176-81dup NP_001305133.1:n.176-83_176-81dup