Canonical Allele Identifier: CA2580074809
Community Standard Title: NM_001378902.1(ROS1):c.5062-46A>C
Gene: ROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117337386T>G , CM000668.2:g.117337386T>G GRCh38
NC_000006.11:g.117658549T>G , CM000668.1:g.117658549T>G GRCh37
NC_000006.10:g.117765242T>G NCBI36
NG_033929.1:g.93470A>C

Transcript Alleles

HGVS Amino-acid Change
NM_001378902.1:c.5062-46A>C MANE Select NP_001365831.1:n.5062-46A>C
ENST00000368507.8:c.5062-46A>C MANE Select ENSP00000357493.3:n.5062-46A>C
NM_001378891.1:c.5068-46A>C NP_001365820.1:n.5068-46A>C
NM_002944.2:c.5080-46A>C NP_002935.2:n.5080-46A>C
NM_002944.3:c.5080-46A>C NP_002935.2:n.5080-46A>C
ENST00000368507.7:c.5062-46A>C ENSP00000357493.3:n.5062-46A>C
ENST00000368508.7:c.5080-46A>C ENSP00000357494.3:n.5080-46A>C
ENST00000467125.1:c.548-15992A>C ENSP00000487717.1:n.548-15992A>C
XM_006715548.2:c.5065-46A>C XP_006715611.1:n.5065-46A>C
XM_006715548.4:c.5065-46A>C XP_006715611.1:n.5065-46A>C
XM_011536049.1:c.5110-46A>C XP_011534351.1:n.5110-46A>C
XM_011536049.2:c.5110-46A>C XP_011534351.1:n.5110-46A>C
XM_011536050.1:c.5107-46A>C XP_011534352.1:n.5107-46A>C
XM_011536050.2:c.5107-46A>C XP_011534352.1:n.5107-46A>C
XM_011536051.1:c.5083-46A>C XP_011534353.1:n.5083-46A>C
XM_011536051.2:c.5083-46A>C XP_011534353.1:n.5083-46A>C
XM_011536052.1:c.5068-46A>C XP_011534354.1:n.5068-46A>C
XM_011536052.2:c.5068-46A>C XP_011534354.1:n.5068-46A>C
XM_011536053.1:c.4936-46A>C XP_011534355.1:n.4936-46A>C
XM_011536053.2:c.4936-46A>C XP_011534355.1:n.4936-46A>C
XM_011536054.1:c.5110-46A>C XP_011534356.1:n.5110-46A>C
XM_011536054.2:c.5110-46A>C XP_011534356.1:n.5110-46A>C
XM_011536055.1:c.5110-46A>C XP_011534357.1:n.5110-46A>C
XM_011536055.2:c.5110-46A>C XP_011534357.1:n.5110-46A>C
XM_011536056.2:c.*2295A>C XP_011534358.1:n.*2295A>C
XM_017011172.1:c.5041-46A>C XP_016866661.1:n.5041-46A>C
XM_017011173.1:c.5038-46A>C XP_016866662.1:n.5038-46A>C