Canonical Allele Identifier: CA373799393

Gene: ROR2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726602C>G , CM000671.2:g.91726602C>G	GRCh38
NC_000009.11:g.94488884C>G , CM000671.1:g.94488884C>G	GRCh37
NC_000009.10:g.93528705C>G	NCBI36
NG_008089.1:g.228561G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1325G>C MANE Select	ENSP00000364860.3:p.Arg442Pro
ENST00000375708.3:c.1325G>C	ENSP00000364860.3:p.Arg442Pro
ENST00000375715.5:c.905G>C	ENSP00000364867.1:p.Arg302Pro
ENST00000550066.5:n.1793G>C
NM_004560.3:c.1325G>C	NP_004551.2:p.Arg442Pro
XM_005252008.3:c.905G>C	XP_005252065.1:p.Arg302Pro
XM_005252009.3:c.122G>C	XP_005252066.1:p.Arg41Pro
XM_006717121.2:c.905G>C	XP_006717184.1:p.Arg302Pro
XM_011518721.1:c.905G>C	XP_011517023.1:p.Arg302Pro
NM_001318204.1:c.1291G>C	NP_001305133.1:p.Asp431His
XM_005252008.4:c.905G>C	XP_005252065.1:p.Arg302Pro
XM_006717121.3:c.905G>C	XP_006717184.1:p.Arg302Pro
XM_017014762.1:c.1316G>C	XP_016870251.1:p.Arg439Pro
XM_017014763.1:c.905G>C	XP_016870252.1:p.Arg302Pro
XR_001746315.1:n.1534G>C
NM_004560.4:c.1325G>C MANE Select	NP_004551.2:p.Arg442Pro
NM_001318204.2:c.1291G>C	NP_001305133.1:p.Asp431His