Canonical Allele Identifier: CA890118

Gene: ROR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.64137548G>A , CM000663.2:g.64137548G>A	GRCh38
NC_000001.10:g.64603231G>A , CM000663.1:g.64603231G>A	GRCh37
NC_000001.9:g.64375819G>A	NCBI36
NG_032801.1:g.368531G>A
NG_032801.2:g.368530G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005012.4:c.610+52G>A MANE Select	NP_005003.2:n.610+52G>A
ENST00000371079.6:c.610+52G>A MANE Select	ENSP00000360120.1:n.610+52G>A
NM_001083592.1:c.610+52G>A	NP_001077061.1:n.610+52G>A
NM_001083592.2:c.610+52G>A	NP_001077061.1:n.610+52G>A
NM_005012.3:c.610+52G>A	NP_005003.2:n.610+52G>A
ENST00000371079.5:c.610+52G>A	ENSP00000360120.1:n.610+52G>A
ENST00000371080.5:c.610+52G>A	ENSP00000360121.1:n.610+52G>A
ENST00000482426.1:n.644+52G>A
ENST00000545203.2:c.445+52G>A	ENSP00000441637.2:n.445+52G>A
XM_011541526.1:c.421+52G>A	XP_011539828.1:n.421+52G>A
XM_017001376.1:c.550+52G>A	XP_016856865.1:n.550+52G>A
XM_017001377.1:c.421+52G>A	XP_016856866.1:n.421+52G>A