Canonical Allele Identifier: CA373799369

Gene: ROR2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726594T>G , CM000671.2:g.91726594T>G	GRCh38
NC_000009.11:g.94488876T>G , CM000671.1:g.94488876T>G	GRCh37
NC_000009.10:g.93528697T>G	NCBI36
NG_008089.1:g.228569A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1333A>C MANE Select	ENSP00000364860.3:p.Met445Leu
ENST00000375708.3:c.1333A>C	ENSP00000364860.3:p.Met445Leu
ENST00000375715.5:c.913A>C	ENSP00000364867.1:p.Met305Leu
ENST00000550066.5:n.1801A>C
NM_004560.3:c.1333A>C	NP_004551.2:p.Met445Leu
XM_005252008.3:c.913A>C	XP_005252065.1:p.Met305Leu
XM_005252009.3:c.130A>C	XP_005252066.1:p.Met44Leu
XM_006717121.2:c.913A>C	XP_006717184.1:p.Met305Leu
XM_011518721.1:c.913A>C	XP_011517023.1:p.Met305Leu
NM_001318204.1:c.1299A>C	NP_001305133.1:p.Ter433Cys
XM_005252008.4:c.913A>C	XP_005252065.1:p.Met305Leu
XM_006717121.3:c.913A>C	XP_006717184.1:p.Met305Leu
XM_017014762.1:c.1324A>C	XP_016870251.1:p.Met442Leu
XM_017014763.1:c.913A>C	XP_016870252.1:p.Met305Leu
XR_001746315.1:n.1542A>C
NM_004560.4:c.1333A>C MANE Select	NP_004551.2:p.Met445Leu
NM_001318204.2:c.1299A>C	NP_001305133.1:p.Ter433Cys