Canonical Allele Identifier: CA2962278985
Gene: ROS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117316944G>A , CM000668.2:g.117316944G>A GRCh38
NC_000006.11:g.117638107G>A , CM000668.1:g.117638107G>A GRCh37
NC_000006.10:g.117744800G>A NCBI36
NG_033929.1:g.113912C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368507.8:c.6117+199C>T MANE Select ENSP00000357493.3:n.6117+199C>T
ENST00000368507.7:c.6117+199C>T ENSP00000357493.3:n.6117+199C>T
ENST00000368508.7:c.6135+199C>T ENSP00000357494.3:n.6135+199C>T
NM_002944.2:c.6135+199C>T NP_002935.2:n.6135+199C>T
XM_006715548.2:c.6120+199C>T XP_006715611.1:n.6120+199C>T
XM_011536049.1:c.6165+199C>T XP_011534351.1:n.6165+199C>T
XM_011536050.1:c.6162+199C>T XP_011534352.1:n.6162+199C>T
XM_011536051.1:c.6138+199C>T XP_011534353.1:n.6138+199C>T
XM_011536052.1:c.6123+199C>T XP_011534354.1:n.6123+199C>T
XM_011536053.1:c.5991+199C>T XP_011534355.1:n.5991+199C>T
XM_011536054.1:c.6165+199C>T XP_011534356.1:n.6165+199C>T
XM_006715548.4:c.6120+199C>T XP_006715611.1:n.6120+199C>T
XM_011536049.2:c.6165+199C>T XP_011534351.1:n.6165+199C>T
XM_011536050.2:c.6162+199C>T XP_011534352.1:n.6162+199C>T
XM_011536051.2:c.6138+199C>T XP_011534353.1:n.6138+199C>T
XM_011536052.2:c.6123+199C>T XP_011534354.1:n.6123+199C>T
XM_011536053.2:c.5991+199C>T XP_011534355.1:n.5991+199C>T
XM_011536054.2:c.6165+199C>T XP_011534356.1:n.6165+199C>T
XM_017011172.1:c.6096+199C>T XP_016866661.1:n.6096+199C>T
XM_017011173.1:c.6093+199C>T XP_016866662.1:n.6093+199C>T
NM_001378891.1:c.6123+199C>T NP_001365820.1:n.6123+199C>T
NM_001378902.1:c.6117+199C>T MANE Select NP_001365831.1:n.6117+199C>T
NM_002944.3:c.6135+199C>T NP_002935.2:n.6135+199C>T
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