Canonical Allele Identifier: CA1657618997
Gene: ROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117301025T= , CM000668.2:g.117301025T= GRCh38
NC_000006.11:g.117622188T= , CM000668.1:g.117622188T= GRCh37
NC_000006.10:g.117728881T= NCBI36
NG_033929.1:g.129831A=

Transcript Alleles

HGVS Amino-acid Change
NM_001378902.1:c.6664A= MANE Select NP_001365831.1:p.Lys2222=
ENST00000368507.8:c.6664A= MANE Select ENSP00000357493.3:p.Lys2222=
NM_001378891.1:c.6670A= NP_001365820.1:p.Lys2224=
NM_002944.2:c.6682A= NP_002935.2:p.Lys2228=
NM_002944.3:c.6682A= NP_002935.2:p.Lys2228=
ENST00000368507.7:c.6664A= ENSP00000357493.3:p.Lys2222=
ENST00000368508.7:c.6682A= ENSP00000357494.3:p.Lys2228=
XM_006715548.2:c.6667A= XP_006715611.1:p.Lys2223=
XM_006715548.4:c.6667A= XP_006715611.1:p.Lys2223=
XM_011536049.1:c.6712A= XP_011534351.1:p.Lys2238=
XM_011536049.2:c.6712A= XP_011534351.1:p.Lys2238=
XM_011536050.1:c.6709A= XP_011534352.1:p.Lys2237=
XM_011536050.2:c.6709A= XP_011534352.1:p.Lys2237=
XM_011536051.1:c.6685A= XP_011534353.1:p.Lys2229=
XM_011536051.2:c.6685A= XP_011534353.1:p.Lys2229=
XM_011536052.1:c.6670A= XP_011534354.1:p.Lys2224=
XM_011536052.2:c.6670A= XP_011534354.1:p.Lys2224=
XM_011536053.1:c.6538A= XP_011534355.1:p.Lys2180=
XM_011536053.2:c.6538A= XP_011534355.1:p.Lys2180=
XM_011536054.1:c.6599+7769A= XP_011534356.1:n.6599+7769A=
XM_011536054.2:c.6599+7769A= XP_011534356.1:n.6599+7769A=
XM_017011172.1:c.6643A= XP_016866661.1:p.Lys2215=
XM_017011173.1:c.6640A= XP_016866662.1:p.Lys2214=