Canonical Allele Identifier: CA1657619058

Gene: ROS1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368507.8:c.6619G= MANE Select	ENSP00000357493.3:p.Asp2207=
ENST00000368507.7:c.6619G=	ENSP00000357493.3:p.Asp2207=
ENST00000368508.7:c.6637G=	ENSP00000357494.3:p.Asp2213=
NM_002944.2:c.6637G=	NP_002935.2:p.Asp2213=
XM_006715548.2:c.6622G=	XP_006715611.1:p.Asp2208=
XM_011536049.1:c.6667G=	XP_011534351.1:p.Asp2223=
XM_011536050.1:c.6664G=	XP_011534352.1:p.Asp2222=
XM_011536051.1:c.6640G=	XP_011534353.1:p.Asp2214=
XM_011536052.1:c.6625G=	XP_011534354.1:p.Asp2209=
XM_011536053.1:c.6493G=	XP_011534355.1:p.Asp2165=
XM_011536054.1:c.6599+7724G=	XP_011534356.1:n.6599+7724G=
XM_006715548.4:c.6622G=	XP_006715611.1:p.Asp2208=
XM_011536049.2:c.6667G=	XP_011534351.1:p.Asp2223=
XM_011536050.2:c.6664G=	XP_011534352.1:p.Asp2222=
XM_011536051.2:c.6640G=	XP_011534353.1:p.Asp2214=
XM_011536052.2:c.6625G=	XP_011534354.1:p.Asp2209=
XM_011536053.2:c.6493G=	XP_011534355.1:p.Asp2165=
XM_011536054.2:c.6599+7724G=	XP_011534356.1:n.6599+7724G=
XM_017011172.1:c.6598G=	XP_016866661.1:p.Asp2200=
XM_017011173.1:c.6595G=	XP_016866662.1:p.Asp2199=
NM_001378891.1:c.6625G=	NP_001365820.1:p.Asp2209=
NM_001378902.1:c.6619G= MANE Select	NP_001365831.1:p.Asp2207=
NM_002944.3:c.6637G=	NP_002935.2:p.Asp2213=