Canonical Allele Identifier: CA373799381

Gene: ROR2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726598C>G , CM000671.2:g.91726598C>G	GRCh38
NC_000009.11:g.94488880C>G , CM000671.1:g.94488880C>G	GRCh37
NC_000009.10:g.93528701C>G	NCBI36
NG_008089.1:g.228565G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1329G>C MANE Select	ENSP00000364860.3:p.Gln443His
ENST00000375708.3:c.1329G>C	ENSP00000364860.3:p.Gln443His
ENST00000375715.5:c.909G>C	ENSP00000364867.1:p.Gln303His
ENST00000550066.5:n.1797G>C
NM_004560.3:c.1329G>C	NP_004551.2:p.Gln443His
XM_005252008.3:c.909G>C	XP_005252065.1:p.Gln303His
XM_005252009.3:c.126G>C	XP_005252066.1:p.Gln42His
XM_006717121.2:c.909G>C	XP_006717184.1:p.Gln303His
XM_011518721.1:c.909G>C	XP_011517023.1:p.Gln303His
NM_001318204.1:c.1295G>C	NP_001305133.1:p.Ser432Thr
XM_005252008.4:c.909G>C	XP_005252065.1:p.Gln303His
XM_006717121.3:c.909G>C	XP_006717184.1:p.Gln303His
XM_017014762.1:c.1320G>C	XP_016870251.1:p.Gln440His
XM_017014763.1:c.909G>C	XP_016870252.1:p.Gln303His
XR_001746315.1:n.1538G>C
NM_004560.4:c.1329G>C MANE Select	NP_004551.2:p.Gln443His
NM_001318204.2:c.1295G>C	NP_001305133.1:p.Ser432Thr