Canonical Allele Identifier: CA16602597
Gene: ROS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 376139
ClinVar RCV Id: RCV000418413
dbSNP Id: rs1057519788
MyVariant Identifiers: chr6:g.117638347C>T (hg19) chr6:g.117317184C>T (hg38)
CIViC: CA16602597
PubMed: PMID:23724914
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117317184C>T , CM000668.2:g.117317184C>T GRCh38
NC_000006.11:g.117638347C>T , CM000668.1:g.117638347C>T GRCh37
NC_000006.10:g.117745040C>T NCBI36
NG_033929.1:g.113672G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368507.8:c.6076G>A MANE Select ENSP00000357493.3:p.Gly2026Arg
ENST00000368507.7:c.6076G>A ENSP00000357493.3:p.Gly2026Arg
ENST00000368508.7:c.6094G>A ENSP00000357494.3:p.Gly2032Arg
NM_002944.2:c.6094G>A NP_002935.2:p.Gly2032Arg
XM_006715548.2:c.6079G>A XP_006715611.1:p.Gly2027Arg
XM_011536049.1:c.6124G>A XP_011534351.1:p.Gly2042Arg
XM_011536050.1:c.6121G>A XP_011534352.1:p.Gly2041Arg
XM_011536051.1:c.6097G>A XP_011534353.1:p.Gly2033Arg
XM_011536052.1:c.6082G>A XP_011534354.1:p.Gly2028Arg
XM_011536053.1:c.5950G>A XP_011534355.1:p.Gly1984Arg
XM_011536054.1:c.6124G>A XP_011534356.1:p.Gly2042Arg
XM_006715548.4:c.6079G>A XP_006715611.1:p.Gly2027Arg
XM_011536049.2:c.6124G>A XP_011534351.1:p.Gly2042Arg
XM_011536050.2:c.6121G>A XP_011534352.1:p.Gly2041Arg
XM_011536051.2:c.6097G>A XP_011534353.1:p.Gly2033Arg
XM_011536052.2:c.6082G>A XP_011534354.1:p.Gly2028Arg
XM_011536053.2:c.5950G>A XP_011534355.1:p.Gly1984Arg
XM_011536054.2:c.6124G>A XP_011534356.1:p.Gly2042Arg
XM_017011172.1:c.6055G>A XP_016866661.1:p.Gly2019Arg
XM_017011173.1:c.6052G>A XP_016866662.1:p.Gly2018Arg
NM_001378891.1:c.6082G>A NP_001365820.1:p.Gly2028Arg
NM_001378902.1:c.6076G>A MANE Select NP_001365831.1:p.Gly2026Arg
NM_002944.3:c.6094G>A NP_002935.2:p.Gly2032Arg
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