Canonical Allele Identifier: CA1657617176

Gene: ROS1

Linked Data

• dbSNP Id: rs1774491325

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.117299208G>A , CM000668.2:g.117299208G>A	GRCh38
NC_000006.11:g.117620371G>A , CM000668.1:g.117620371G>A	GRCh37
NC_000006.10:g.117727064G>A	NCBI36
NG_033929.1:g.131648C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368507.8:c.6715+1766C>T MANE Select	ENSP00000357493.3:n.6715+1766C>T
ENST00000368507.7:c.6715+1766C>T	ENSP00000357493.3:n.6715+1766C>T
ENST00000368508.7:c.6733+1766C>T	ENSP00000357494.3:n.6733+1766C>T
NM_002944.2:c.6733+1766C>T	NP_002935.2:n.6733+1766C>T
XM_006715548.2:c.6718+1766C>T	XP_006715611.1:n.6718+1766C>T
XM_011536049.1:c.6763+1766C>T	XP_011534351.1:n.6763+1766C>T
XM_011536050.1:c.6760+1766C>T	XP_011534352.1:n.6760+1766C>T
XM_011536051.1:c.6736+1766C>T	XP_011534353.1:n.6736+1766C>T
XM_011536052.1:c.6721+1766C>T	XP_011534354.1:n.6721+1766C>T
XM_011536053.1:c.6589+1766C>T	XP_011534355.1:n.6589+1766C>T
XM_011536054.1:c.6599+9586C>T	XP_011534356.1:n.6599+9586C>T
XM_006715548.4:c.6718+1766C>T	XP_006715611.1:n.6718+1766C>T
XM_011536049.2:c.6763+1766C>T	XP_011534351.1:n.6763+1766C>T
XM_011536050.2:c.6760+1766C>T	XP_011534352.1:n.6760+1766C>T
XM_011536051.2:c.6736+1766C>T	XP_011534353.1:n.6736+1766C>T
XM_011536052.2:c.6721+1766C>T	XP_011534354.1:n.6721+1766C>T
XM_011536053.2:c.6589+1766C>T	XP_011534355.1:n.6589+1766C>T
XM_011536054.2:c.6599+9586C>T	XP_011534356.1:n.6599+9586C>T
XM_017011172.1:c.6694+1766C>T	XP_016866661.1:n.6694+1766C>T
XM_017011173.1:c.6691+1766C>T	XP_016866662.1:n.6691+1766C>T
NM_001378891.1:c.6721+1766C>T	NP_001365820.1:n.6721+1766C>T
NM_001378902.1:c.6715+1766C>T MANE Select	NP_001365831.1:n.6715+1766C>T
NM_002944.3:c.6733+1766C>T	NP_002935.2:n.6733+1766C>T