Canonical Allele Identifier: CA5120872

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91733196G>A , CM000671.2:g.91733196G>A	GRCh38
NC_000009.11:g.94495478G>A , CM000671.1:g.94495478G>A	GRCh37
NC_000009.10:g.93535299G>A	NCBI36
NG_008089.1:g.221967C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.863C>T MANE Select	ENSP00000364860.3:p.Ala288Val
ENST00000375708.3:c.863C>T	ENSP00000364860.3:p.Ala288Val
ENST00000375715.5:c.443C>T	ENSP00000364867.1:p.Ala148Val
ENST00000550066.5:n.1331C>T
NM_004560.3:c.863C>T	NP_004551.2:p.Ala288Val
XM_005252008.3:c.443C>T	XP_005252065.1:p.Ala148Val
XM_006717121.2:c.443C>T	XP_006717184.1:p.Ala148Val
XM_011518721.1:c.443C>T	XP_011517023.1:p.Ala148Val
NM_001318204.1:c.863C>T	NP_001305133.1:p.Ala288Val
XM_005252008.4:c.443C>T	XP_005252065.1:p.Ala148Val
XM_006717121.3:c.443C>T	XP_006717184.1:p.Ala148Val
XM_017014762.1:c.854C>T	XP_016870251.1:p.Ala285Val
XM_017014763.1:c.443C>T	XP_016870252.1:p.Ala148Val
XR_001746315.1:n.1106C>T
NM_004560.4:c.863C>T MANE Select	NP_004551.2:p.Ala288Val
NM_001318204.2:c.863C>T	NP_001305133.1:p.Ala288Val