Canonical Allele Identifier: CA373796451

Gene: ROR2

Linked Data

• COSMIC: COSM1581608
• MyVariant Identifiers: chr9:g.94486747A>G (hg19) ; chr9:g.91724465A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724465A>G , CM000671.2:g.91724465A>G	GRCh38
NC_000009.11:g.94486747A>G , CM000671.1:g.94486747A>G	GRCh37
NC_000009.10:g.93526568A>G	NCBI36
NG_008089.1:g.230698T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2029T>C MANE Select	ENSP00000364860.3:p.Ser677Pro
ENST00000375708.3:c.2029T>C	ENSP00000364860.3:p.Ser677Pro
ENST00000375715.5:c.1609T>C	ENSP00000364867.1:p.Ser537Pro
ENST00000550066.5:n.2497T>C
NM_004560.3:c.2029T>C	NP_004551.2:p.Ser677Pro
XM_005252008.3:c.1609T>C	XP_005252065.1:p.Ser537Pro
XM_005252009.3:c.826T>C	XP_005252066.1:p.Ser276Pro
XM_006717121.2:c.1609T>C	XP_006717184.1:p.Ser537Pro
XM_011518721.1:c.1609T>C	XP_011517023.1:p.Ser537Pro
XM_005252008.4:c.1609T>C	XP_005252065.1:p.Ser537Pro
XM_006717121.3:c.1609T>C	XP_006717184.1:p.Ser537Pro
XM_017014762.1:c.2020T>C	XP_016870251.1:p.Ser674Pro
XM_017014763.1:c.1609T>C	XP_016870252.1:p.Ser537Pro
NM_004560.4:c.2029T>C MANE Select	NP_004551.2:p.Ser677Pro