Canonical Allele Identifier: CA365439758

Gene: ROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.117301070C>A , CM000668.2:g.117301070C>A	GRCh38
NC_000006.11:g.117622233C>A , CM000668.1:g.117622233C>A	GRCh37
NC_000006.10:g.117728926C>A	NCBI36
NG_033929.1:g.129786G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368507.8:c.6619G>T MANE Select	ENSP00000357493.3:p.Asp2207Tyr
ENST00000368507.7:c.6619G>T	ENSP00000357493.3:p.Asp2207Tyr
ENST00000368508.7:c.6637G>T	ENSP00000357494.3:p.Asp2213Tyr
NM_002944.2:c.6637G>T	NP_002935.2:p.Asp2213Tyr
XM_006715548.2:c.6622G>T	XP_006715611.1:p.Asp2208Tyr
XM_011536049.1:c.6667G>T	XP_011534351.1:p.Asp2223Tyr
XM_011536050.1:c.6664G>T	XP_011534352.1:p.Asp2222Tyr
XM_011536051.1:c.6640G>T	XP_011534353.1:p.Asp2214Tyr
XM_011536052.1:c.6625G>T	XP_011534354.1:p.Asp2209Tyr
XM_011536053.1:c.6493G>T	XP_011534355.1:p.Asp2165Tyr
XM_011536054.1:c.6599+7724G>T	XP_011534356.1:n.6599+7724G>T
XM_006715548.4:c.6622G>T	XP_006715611.1:p.Asp2208Tyr
XM_011536049.2:c.6667G>T	XP_011534351.1:p.Asp2223Tyr
XM_011536050.2:c.6664G>T	XP_011534352.1:p.Asp2222Tyr
XM_011536051.2:c.6640G>T	XP_011534353.1:p.Asp2214Tyr
XM_011536052.2:c.6625G>T	XP_011534354.1:p.Asp2209Tyr
XM_011536053.2:c.6493G>T	XP_011534355.1:p.Asp2165Tyr
XM_011536054.2:c.6599+7724G>T	XP_011534356.1:n.6599+7724G>T
XM_017011172.1:c.6598G>T	XP_016866661.1:p.Asp2200Tyr
XM_017011173.1:c.6595G>T	XP_016866662.1:p.Asp2199Tyr
NM_001378891.1:c.6625G>T	NP_001365820.1:p.Asp2209Tyr
NM_001378902.1:c.6619G>T MANE Select	NP_001365831.1:p.Asp2207Tyr
NM_002944.3:c.6637G>T	NP_002935.2:p.Asp2213Tyr