Canonical Allele Identifier: CA373799376

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94488879G>C (hg19) ; chr9:g.91726597G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726597G>C , CM000671.2:g.91726597G>C	GRCh38
NC_000009.11:g.94488879G>C , CM000671.1:g.94488879G>C	GRCh37
NC_000009.10:g.93528700G>C	NCBI36
NG_008089.1:g.228566C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1330C>G MANE Select	ENSP00000364860.3:p.Leu444Val
ENST00000375708.3:c.1330C>G	ENSP00000364860.3:p.Leu444Val
ENST00000375715.5:c.910C>G	ENSP00000364867.1:p.Leu304Val
ENST00000550066.5:n.1798C>G
NM_004560.3:c.1330C>G	NP_004551.2:p.Leu444Val
XM_005252008.3:c.910C>G	XP_005252065.1:p.Leu304Val
XM_005252009.3:c.127C>G	XP_005252066.1:p.Leu43Val
XM_006717121.2:c.910C>G	XP_006717184.1:p.Leu304Val
XM_011518721.1:c.910C>G	XP_011517023.1:p.Leu304Val
NM_001318204.1:c.1296C>G	NP_001305133.1:p.Ser432Arg
XM_005252008.4:c.910C>G	XP_005252065.1:p.Leu304Val
XM_006717121.3:c.910C>G	XP_006717184.1:p.Leu304Val
XM_017014762.1:c.1321C>G	XP_016870251.1:p.Leu441Val
XM_017014763.1:c.910C>G	XP_016870252.1:p.Leu304Val
XR_001746315.1:n.1539C>G
NM_004560.4:c.1330C>G MANE Select	NP_004551.2:p.Leu444Val
NM_001318204.2:c.1296C>G	NP_001305133.1:p.Ser432Arg