Canonical Allele Identifier: CA365440890
Gene: ROS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117317145T>G , CM000668.2:g.117317145T>G GRCh38
NC_000006.11:g.117638308T>G , CM000668.1:g.117638308T>G GRCh37
NC_000006.10:g.117745001T>G NCBI36
NG_033929.1:g.113711A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368507.8:c.6115A>C MANE Select ENSP00000357493.3:p.Thr2039Pro
ENST00000368507.7:c.6115A>C ENSP00000357493.3:p.Thr2039Pro
ENST00000368508.7:c.6133A>C ENSP00000357494.3:p.Thr2045Pro
NM_002944.2:c.6133A>C NP_002935.2:p.Thr2045Pro
XM_006715548.2:c.6118A>C XP_006715611.1:p.Thr2040Pro
XM_011536049.1:c.6163A>C XP_011534351.1:p.Thr2055Pro
XM_011536050.1:c.6160A>C XP_011534352.1:p.Thr2054Pro
XM_011536051.1:c.6136A>C XP_011534353.1:p.Thr2046Pro
XM_011536052.1:c.6121A>C XP_011534354.1:p.Thr2041Pro
XM_011536053.1:c.5989A>C XP_011534355.1:p.Thr1997Pro
XM_011536054.1:c.6163A>C XP_011534356.1:p.Thr2055Pro
XM_006715548.4:c.6118A>C XP_006715611.1:p.Thr2040Pro
XM_011536049.2:c.6163A>C XP_011534351.1:p.Thr2055Pro
XM_011536050.2:c.6160A>C XP_011534352.1:p.Thr2054Pro
XM_011536051.2:c.6136A>C XP_011534353.1:p.Thr2046Pro
XM_011536052.2:c.6121A>C XP_011534354.1:p.Thr2041Pro
XM_011536053.2:c.5989A>C XP_011534355.1:p.Thr1997Pro
XM_011536054.2:c.6163A>C XP_011534356.1:p.Thr2055Pro
XM_017011172.1:c.6094A>C XP_016866661.1:p.Thr2032Pro
XM_017011173.1:c.6091A>C XP_016866662.1:p.Thr2031Pro
NM_001378891.1:c.6121A>C NP_001365820.1:p.Thr2041Pro
NM_001378902.1:c.6115A>C MANE Select NP_001365831.1:p.Thr2039Pro
NM_002944.3:c.6133A>C NP_002935.2:p.Thr2045Pro
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