Canonical Allele Identifier: CA365441006
Gene: ROS1 HGNC NCBI

Linked Data

dbSNP Id: rs2128555610
MyVariant Identifiers: chr6:g.117638365G>T (hg19) chr6:g.117317202G>T (hg38)
CIViC: CA365441006
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117317202G>T , CM000668.2:g.117317202G>T GRCh38
NC_000006.11:g.117638365G>T , CM000668.1:g.117638365G>T GRCh37
NC_000006.10:g.117745058G>T NCBI36
NG_033929.1:g.113654C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368507.8:c.6058C>A MANE Select ENSP00000357493.3:p.Leu2020Met
ENST00000368507.7:c.6058C>A ENSP00000357493.3:p.Leu2020Met
ENST00000368508.7:c.6076C>A ENSP00000357494.3:p.Leu2026Met
NM_002944.2:c.6076C>A NP_002935.2:p.Leu2026Met
XM_006715548.2:c.6061C>A XP_006715611.1:p.Leu2021Met
XM_011536049.1:c.6106C>A XP_011534351.1:p.Leu2036Met
XM_011536050.1:c.6103C>A XP_011534352.1:p.Leu2035Met
XM_011536051.1:c.6079C>A XP_011534353.1:p.Leu2027Met
XM_011536052.1:c.6064C>A XP_011534354.1:p.Leu2022Met
XM_011536053.1:c.5932C>A XP_011534355.1:p.Leu1978Met
XM_011536054.1:c.6106C>A XP_011534356.1:p.Leu2036Met
XM_006715548.4:c.6061C>A XP_006715611.1:p.Leu2021Met
XM_011536049.2:c.6106C>A XP_011534351.1:p.Leu2036Met
XM_011536050.2:c.6103C>A XP_011534352.1:p.Leu2035Met
XM_011536051.2:c.6079C>A XP_011534353.1:p.Leu2027Met
XM_011536052.2:c.6064C>A XP_011534354.1:p.Leu2022Met
XM_011536053.2:c.5932C>A XP_011534355.1:p.Leu1978Met
XM_011536054.2:c.6106C>A XP_011534356.1:p.Leu2036Met
XM_017011172.1:c.6037C>A XP_016866661.1:p.Leu2013Met
XM_017011173.1:c.6034C>A XP_016866662.1:p.Leu2012Met
NM_001378891.1:c.6064C>A NP_001365820.1:p.Leu2022Met
NM_001378902.1:c.6058C>A MANE Select NP_001365831.1:p.Leu2020Met
NM_002944.3:c.6076C>A NP_002935.2:p.Leu2026Met
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