Canonical Allele Identifier: CA890016
Gene: ROR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64049707C>T , CM000663.2:g.64049707C>T GRCh38
NC_000001.10:g.64515379C>T , CM000663.1:g.64515379C>T GRCh37
NC_000001.9:g.64287967C>T NCBI36
NG_032801.1:g.280690C>T
NG_032801.2:g.280689C>T

Transcript Alleles

HGVS Amino-acid Change
NM_005012.4:c.180C>T MANE Select NP_005003.2:p.Leu60=
ENST00000371079.6:c.180C>T MANE Select ENSP00000360120.1:p.Leu60=
NM_001083592.1:c.180C>T NP_001077061.1:p.Leu60=
NM_001083592.2:c.180C>T NP_001077061.1:p.Leu60=
NM_005012.3:c.180C>T NP_005003.2:p.Leu60=
ENST00000371079.5:c.180C>T ENSP00000360120.1:p.Leu60=
ENST00000371080.5:c.180C>T ENSP00000360121.1:p.Leu60=
ENST00000482426.1:n.214C>T
ENST00000545203.2:c.15C>T ENSP00000441637.2:p.Leu5=
XM_011541526.1:c.-10C>T XP_011539828.1:n.-10C>T
XM_017001376.1:c.120C>T XP_016856865.1:p.Leu40=
XM_017001377.1:c.-10C>T XP_016856866.1:n.-10C>T