Canonical Allele Identifier: CA365439647

Gene: ROS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.117301021G>T , CM000668.2:g.117301021G>T	GRCh38
NC_000006.11:g.117622184G>T , CM000668.1:g.117622184G>T	GRCh37
NC_000006.10:g.117728877G>T	NCBI36
NG_033929.1:g.129835C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368507.8:c.6668C>A MANE Select	ENSP00000357493.3:p.Ser2223Tyr
ENST00000368507.7:c.6668C>A	ENSP00000357493.3:p.Ser2223Tyr
ENST00000368508.7:c.6686C>A	ENSP00000357494.3:p.Ser2229Tyr
NM_002944.2:c.6686C>A	NP_002935.2:p.Ser2229Tyr
XM_006715548.2:c.6671C>A	XP_006715611.1:p.Ser2224Tyr
XM_011536049.1:c.6716C>A	XP_011534351.1:p.Ser2239Tyr
XM_011536050.1:c.6713C>A	XP_011534352.1:p.Ser2238Tyr
XM_011536051.1:c.6689C>A	XP_011534353.1:p.Ser2230Tyr
XM_011536052.1:c.6674C>A	XP_011534354.1:p.Ser2225Tyr
XM_011536053.1:c.6542C>A	XP_011534355.1:p.Ser2181Tyr
XM_011536054.1:c.6599+7773C>A	XP_011534356.1:n.6599+7773C>A
XM_006715548.4:c.6671C>A	XP_006715611.1:p.Ser2224Tyr
XM_011536049.2:c.6716C>A	XP_011534351.1:p.Ser2239Tyr
XM_011536050.2:c.6713C>A	XP_011534352.1:p.Ser2238Tyr
XM_011536051.2:c.6689C>A	XP_011534353.1:p.Ser2230Tyr
XM_011536052.2:c.6674C>A	XP_011534354.1:p.Ser2225Tyr
XM_011536053.2:c.6542C>A	XP_011534355.1:p.Ser2181Tyr
XM_011536054.2:c.6599+7773C>A	XP_011534356.1:n.6599+7773C>A
XM_017011172.1:c.6647C>A	XP_016866661.1:p.Ser2216Tyr
XM_017011173.1:c.6644C>A	XP_016866662.1:p.Ser2215Tyr
NM_001378891.1:c.6674C>A	NP_001365820.1:p.Ser2225Tyr
NM_001378902.1:c.6668C>A MANE Select	NP_001365831.1:p.Ser2223Tyr
NM_002944.3:c.6686C>A	NP_002935.2:p.Ser2229Tyr