Canonical Allele Identifier: CA5120515

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724499C>G , CM000671.2:g.91724499C>G	GRCh38
NC_000009.11:g.94486781C>G , CM000671.1:g.94486781C>G	GRCh37
NC_000009.10:g.93526602C>G	NCBI36
NG_008089.1:g.230664G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.1995G>C MANE Select	NP_004551.2:p.Met665Ile
ENST00000375708.4:c.1995G>C MANE Select	ENSP00000364860.3:p.Met665Ile
NM_004560.3:c.1995G>C	NP_004551.2:p.Met665Ile
ENST00000375708.3:c.1995G>C	ENSP00000364860.3:p.Met665Ile
ENST00000375715.5:c.1575G>C	ENSP00000364867.1:p.Met525Ile
ENST00000550066.5:n.2463G>C
XM_005252008.3:c.1575G>C	XP_005252065.1:p.Met525Ile
XM_005252008.4:c.1575G>C	XP_005252065.1:p.Met525Ile
XM_005252009.3:c.792G>C	XP_005252066.1:p.Met264Ile
XM_006717121.2:c.1575G>C	XP_006717184.1:p.Met525Ile
XM_006717121.3:c.1575G>C	XP_006717184.1:p.Met525Ile
XM_011518721.1:c.1575G>C	XP_011517023.1:p.Met525Ile
XM_017014762.1:c.1986G>C	XP_016870251.1:p.Met662Ile
XM_017014763.1:c.1575G>C	XP_016870252.1:p.Met525Ile