Canonical Allele Identifier: CA5120369

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723973G>C , CM000671.2:g.91723973G>C	GRCh38
NC_000009.11:g.94486255G>C , CM000671.1:g.94486255G>C	GRCh37
NC_000009.10:g.93526076G>C	NCBI36
NG_008089.1:g.231190C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.2521C>G MANE Select	NP_004551.2:p.Gln841Glu
ENST00000375708.4:c.2521C>G MANE Select	ENSP00000364860.3:p.Gln841Glu
NM_004560.3:c.2521C>G	NP_004551.2:p.Gln841Glu
ENST00000375708.3:c.2521C>G	ENSP00000364860.3:p.Gln841Glu
ENST00000375715.5:c.1920+181C>G	ENSP00000364867.1:n.1920+181C>G
ENST00000550066.5:n.2989C>G
XM_005252008.3:c.2101C>G	XP_005252065.1:p.Gln701Glu
XM_005252008.4:c.2101C>G	XP_005252065.1:p.Gln701Glu
XM_005252009.3:c.1318C>G	XP_005252066.1:p.Gln440Glu
XM_006717121.2:c.2101C>G	XP_006717184.1:p.Gln701Glu
XM_006717121.3:c.2101C>G	XP_006717184.1:p.Gln701Glu
XM_011518721.1:c.2101C>G	XP_011517023.1:p.Gln701Glu
XM_017014762.1:c.2512C>G	XP_016870251.1:p.Gln838Glu
XM_017014763.1:c.2101C>G	XP_016870252.1:p.Gln701Glu