Canonical Allele Identifier: CA365444218

Gene: ROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.117397039G>C , CM000668.2:g.117397039G>C	GRCh38
NC_000006.11:g.117718202G>C , CM000668.1:g.117718202G>C	GRCh37
NC_000006.10:g.117824895G>C	NCBI36
NG_033929.1:g.33817C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001378902.1:c.682C>G MANE Select	NP_001365831.1:p.Gln228Glu
ENST00000368507.8:c.682C>G MANE Select	ENSP00000357493.3:p.Gln228Glu
NM_001378891.1:c.682C>G	NP_001365820.1:p.Gln228Glu
NM_002944.2:c.655C>G	NP_002935.2:p.Gln219Glu
NM_002944.3:c.655C>G	NP_002935.2:p.Gln219Glu
ENST00000368507.7:c.682C>G	ENSP00000357493.3:p.Gln228Glu
ENST00000368508.7:c.655C>G	ENSP00000357494.3:p.Gln219Glu
ENST00000467125.1:c.548-75645C>G	ENSP00000487717.1:n.548-75645C>G
XM_006715548.2:c.682C>G	XP_006715611.1:p.Gln228Glu
XM_006715548.4:c.682C>G	XP_006715611.1:p.Gln228Glu
XM_011536049.1:c.682C>G	XP_011534351.1:p.Gln228Glu
XM_011536049.2:c.682C>G	XP_011534351.1:p.Gln228Glu
XM_011536050.1:c.682C>G	XP_011534352.1:p.Gln228Glu
XM_011536050.2:c.682C>G	XP_011534352.1:p.Gln228Glu
XM_011536051.1:c.655C>G	XP_011534353.1:p.Gln219Glu
XM_011536051.2:c.655C>G	XP_011534353.1:p.Gln219Glu
XM_011536052.1:c.682C>G	XP_011534354.1:p.Gln228Glu
XM_011536052.2:c.682C>G	XP_011534354.1:p.Gln228Glu
XM_011536053.1:c.682C>G	XP_011534355.1:p.Gln228Glu
XM_011536053.2:c.682C>G	XP_011534355.1:p.Gln228Glu
XM_011536054.1:c.682C>G	XP_011534356.1:p.Gln228Glu
XM_011536054.2:c.682C>G	XP_011534356.1:p.Gln228Glu
XM_011536055.1:c.682C>G	XP_011534357.1:p.Gln228Glu
XM_011536055.2:c.682C>G	XP_011534357.1:p.Gln228Glu
XM_011536056.1:c.682C>G	XP_011534358.1:p.Gln228Glu
XM_011536056.2:c.682C>G	XP_011534358.1:p.Gln228Glu
XM_011536057.1:c.682C>G	XP_011534359.1:p.Gln228Glu
XM_011536057.3:c.682C>G	XP_011534359.1:p.Gln228Glu
XM_011536058.1:c.682C>G	XP_011534360.1:p.Gln228Glu
XM_011536058.2:c.682C>G	XP_011534360.1:p.Gln228Glu
XM_017011172.1:c.655C>G	XP_016866661.1:p.Gln219Glu
XM_017011173.1:c.655C>G	XP_016866662.1:p.Gln219Glu