Canonical Allele Identifier: CA373800040

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91730993T>A , CM000671.2:g.91730993T>A	GRCh38
NC_000009.11:g.94493275T>A , CM000671.1:g.94493275T>A	GRCh37
NC_000009.10:g.93533096T>A	NCBI36
NG_008089.1:g.224170A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.1100A>T MANE Select	NP_004551.2:p.Asn367Ile
ENST00000375708.4:c.1100A>T MANE Select	ENSP00000364860.3:p.Asn367Ile
NM_001318204.1:c.1100A>T	NP_001305133.1:p.Asn367Ile
NM_001318204.2:c.1100A>T	NP_001305133.1:p.Asn367Ile
NM_004560.3:c.1100A>T	NP_004551.2:p.Asn367Ile
ENST00000375708.3:c.1100A>T	ENSP00000364860.3:p.Asn367Ile
ENST00000375715.5:c.680A>T	ENSP00000364867.1:p.Asn227Ile
ENST00000550066.5:n.1568A>T
XM_005252008.3:c.680A>T	XP_005252065.1:p.Asn227Ile
XM_005252008.4:c.680A>T	XP_005252065.1:p.Asn227Ile
XM_005252009.3:c.-70A>T	XP_005252066.1:n.-70A>T
XM_006717121.2:c.680A>T	XP_006717184.1:p.Asn227Ile
XM_006717121.3:c.680A>T	XP_006717184.1:p.Asn227Ile
XM_011518721.1:c.680A>T	XP_011517023.1:p.Asn227Ile
XM_017014762.1:c.1091A>T	XP_016870251.1:p.Asn364Ile
XM_017014763.1:c.680A>T	XP_016870252.1:p.Asn227Ile
XR_001746315.1:n.1343A>T