Canonical Allele Identifier: CA373798352

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724978T>A , CM000671.2:g.91724978T>A	GRCh38
NC_000009.11:g.94487260T>A , CM000671.1:g.94487260T>A	GRCh37
NC_000009.10:g.93527081T>A	NCBI36
NG_008089.1:g.230185A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.1516A>T MANE Select	NP_004551.2:p.Ile506Phe
ENST00000375708.4:c.1516A>T MANE Select	ENSP00000364860.3:p.Ile506Phe
NM_004560.3:c.1516A>T	NP_004551.2:p.Ile506Phe
ENST00000375708.3:c.1516A>T	ENSP00000364860.3:p.Ile506Phe
ENST00000375715.5:c.1096A>T	ENSP00000364867.1:p.Ile366Phe
ENST00000550066.5:n.1984A>T
XM_005252008.3:c.1096A>T	XP_005252065.1:p.Ile366Phe
XM_005252008.4:c.1096A>T	XP_005252065.1:p.Ile366Phe
XM_005252009.3:c.313A>T	XP_005252066.1:p.Ile105Phe
XM_006717121.2:c.1096A>T	XP_006717184.1:p.Ile366Phe
XM_006717121.3:c.1096A>T	XP_006717184.1:p.Ile366Phe
XM_011518721.1:c.1096A>T	XP_011517023.1:p.Ile366Phe
XM_017014762.1:c.1507A>T	XP_016870251.1:p.Ile503Phe
XM_017014763.1:c.1096A>T	XP_016870252.1:p.Ile366Phe