Canonical Allele Identifier: CA373800691

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91733160C>A , CM000671.2:g.91733160C>A	GRCh38
NC_000009.11:g.94495442C>A , CM000671.1:g.94495442C>A	GRCh37
NC_000009.10:g.93535263C>A	NCBI36
NG_008089.1:g.222003G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.899G>T MANE Select	NP_004551.2:p.Cys300Phe
ENST00000375708.4:c.899G>T MANE Select	ENSP00000364860.3:p.Cys300Phe
NM_001318204.1:c.899G>T	NP_001305133.1:p.Cys300Phe
NM_001318204.2:c.899G>T	NP_001305133.1:p.Cys300Phe
NM_004560.3:c.899G>T	NP_004551.2:p.Cys300Phe
ENST00000375708.3:c.899G>T	ENSP00000364860.3:p.Cys300Phe
ENST00000375715.5:c.479G>T	ENSP00000364867.1:p.Cys160Phe
ENST00000550066.5:n.1367G>T
XM_005252008.3:c.479G>T	XP_005252065.1:p.Cys160Phe
XM_005252008.4:c.479G>T	XP_005252065.1:p.Cys160Phe
XM_006717121.2:c.479G>T	XP_006717184.1:p.Cys160Phe
XM_006717121.3:c.479G>T	XP_006717184.1:p.Cys160Phe
XM_011518721.1:c.479G>T	XP_011517023.1:p.Cys160Phe
XM_017014762.1:c.890G>T	XP_016870251.1:p.Cys297Phe
XM_017014763.1:c.479G>T	XP_016870252.1:p.Cys160Phe
XR_001746315.1:n.1142G>T