Canonical Allele Identifier: CA5120728

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726610C>T , CM000671.2:g.91726610C>T	GRCh38
NC_000009.11:g.94488892C>T , CM000671.1:g.94488892C>T	GRCh37
NC_000009.10:g.93528713C>T	NCBI36
NG_008089.1:g.228553G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.1317G>A MANE Select	NP_004551.2:p.Pro439=
ENST00000375708.4:c.1317G>A MANE Select	ENSP00000364860.3:p.Pro439=
NM_001318204.1:c.1283G>A	NP_001305133.1:p.Arg428His
NM_001318204.2:c.1283G>A	NP_001305133.1:p.Arg428His
NM_004560.3:c.1317G>A	NP_004551.2:p.Pro439=
ENST00000375708.3:c.1317G>A	ENSP00000364860.3:p.Pro439=
ENST00000375715.5:c.897G>A	ENSP00000364867.1:p.Pro299=
ENST00000550066.5:n.1785G>A
XM_005252008.3:c.897G>A	XP_005252065.1:p.Pro299=
XM_005252008.4:c.897G>A	XP_005252065.1:p.Pro299=
XM_005252009.3:c.114G>A	XP_005252066.1:p.Pro38=
XM_006717121.2:c.897G>A	XP_006717184.1:p.Pro299=
XM_006717121.3:c.897G>A	XP_006717184.1:p.Pro299=
XM_011518721.1:c.897G>A	XP_011517023.1:p.Pro299=
XM_017014762.1:c.1308G>A	XP_016870251.1:p.Pro436=
XM_017014763.1:c.897G>A	XP_016870252.1:p.Pro299=
XR_001746315.1:n.1526G>A