Canonical Allele Identifier: CA145987575
Gene: ROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117403216C>A , CM000668.2:g.117403216C>A GRCh38
NC_000006.11:g.117724379C>A , CM000668.1:g.117724379C>A GRCh37
NC_000006.10:g.117831072C>A NCBI36
NG_033929.1:g.27640G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368507.8:c.527G>T MANE Select ENSP00000357493.3:p.Arg176Leu
ENST00000368507.7:c.527G>T ENSP00000357493.3:p.Arg176Leu
ENST00000368508.7:c.500G>T ENSP00000357494.3:p.Arg167Leu
ENST00000467125.1:c.548-81822G>T ENSP00000487717.1:n.548-81822G>T
NM_002944.2:c.500G>T NP_002935.2:p.Arg167Leu
XM_006715548.2:c.527G>T XP_006715611.1:p.Arg176Leu
XM_011536049.1:c.527G>T XP_011534351.1:p.Arg176Leu
XM_011536050.1:c.527G>T XP_011534352.1:p.Arg176Leu
XM_011536051.1:c.500G>T XP_011534353.1:p.Arg167Leu
XM_011536052.1:c.527G>T XP_011534354.1:p.Arg176Leu
XM_011536053.1:c.527G>T XP_011534355.1:p.Arg176Leu
XM_011536054.1:c.527G>T XP_011534356.1:p.Arg176Leu
XM_011536055.1:c.527G>T XP_011534357.1:p.Arg176Leu
XM_011536056.1:c.527G>T XP_011534358.1:p.Arg176Leu
XM_011536057.1:c.527G>T XP_011534359.1:p.Arg176Leu
XM_011536058.1:c.527G>T XP_011534360.1:p.Arg176Leu
XM_006715548.4:c.527G>T XP_006715611.1:p.Arg176Leu
XM_011536049.2:c.527G>T XP_011534351.1:p.Arg176Leu
XM_011536050.2:c.527G>T XP_011534352.1:p.Arg176Leu
XM_011536051.2:c.500G>T XP_011534353.1:p.Arg167Leu
XM_011536052.2:c.527G>T XP_011534354.1:p.Arg176Leu
XM_011536053.2:c.527G>T XP_011534355.1:p.Arg176Leu
XM_011536054.2:c.527G>T XP_011534356.1:p.Arg176Leu
XM_011536055.2:c.527G>T XP_011534357.1:p.Arg176Leu
XM_011536056.2:c.527G>T XP_011534358.1:p.Arg176Leu
XM_011536057.3:c.527G>T XP_011534359.1:p.Arg176Leu
XM_011536058.2:c.527G>T XP_011534360.1:p.Arg176Leu
XM_017011172.1:c.500G>T XP_016866661.1:p.Arg167Leu
XM_017011173.1:c.500G>T XP_016866662.1:p.Arg167Leu
NM_001378891.1:c.527G>T NP_001365820.1:p.Arg176Leu
NM_001378902.1:c.527G>T MANE Select NP_001365831.1:p.Arg176Leu
NM_002944.3:c.500G>T NP_002935.2:p.Arg167Leu