Canonical Allele Identifier: CA3974153
Gene: ROS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117317148C>T , CM000668.2:g.117317148C>T GRCh38
NC_000006.11:g.117638311C>T , CM000668.1:g.117638311C>T GRCh37
NC_000006.10:g.117745004C>T NCBI36
NG_033929.1:g.113708G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368507.8:c.6112G>A MANE Select ENSP00000357493.3:p.Ala2038Thr
ENST00000368507.7:c.6112G>A ENSP00000357493.3:p.Ala2038Thr
ENST00000368508.7:c.6130G>A ENSP00000357494.3:p.Ala2044Thr
NM_002944.2:c.6130G>A NP_002935.2:p.Ala2044Thr
XM_006715548.2:c.6115G>A XP_006715611.1:p.Ala2039Thr
XM_011536049.1:c.6160G>A XP_011534351.1:p.Ala2054Thr
XM_011536050.1:c.6157G>A XP_011534352.1:p.Ala2053Thr
XM_011536051.1:c.6133G>A XP_011534353.1:p.Ala2045Thr
XM_011536052.1:c.6118G>A XP_011534354.1:p.Ala2040Thr
XM_011536053.1:c.5986G>A XP_011534355.1:p.Ala1996Thr
XM_011536054.1:c.6160G>A XP_011534356.1:p.Ala2054Thr
XM_006715548.4:c.6115G>A XP_006715611.1:p.Ala2039Thr
XM_011536049.2:c.6160G>A XP_011534351.1:p.Ala2054Thr
XM_011536050.2:c.6157G>A XP_011534352.1:p.Ala2053Thr
XM_011536051.2:c.6133G>A XP_011534353.1:p.Ala2045Thr
XM_011536052.2:c.6118G>A XP_011534354.1:p.Ala2040Thr
XM_011536053.2:c.5986G>A XP_011534355.1:p.Ala1996Thr
XM_011536054.2:c.6160G>A XP_011534356.1:p.Ala2054Thr
XM_017011172.1:c.6091G>A XP_016866661.1:p.Ala2031Thr
XM_017011173.1:c.6088G>A XP_016866662.1:p.Ala2030Thr
NM_001378891.1:c.6118G>A NP_001365820.1:p.Ala2040Thr
NM_001378902.1:c.6112G>A MANE Select NP_001365831.1:p.Ala2038Thr
NM_002944.3:c.6130G>A NP_002935.2:p.Ala2044Thr
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