Canonical Allele Identifier: CA2507755036
Gene: ETS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.38823560_38823561insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA , CM000683.2:g.38823560_38823561insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA GRCh38
NC_000021.8:g.40195484_40195485insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA , CM000683.1:g.40195484_40195485insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA GRCh37
NC_000021.7:g.39117354_39117355insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360214.8:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA ENSP00000353344.3:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTG...
ENST00000360938.8:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA MANE Select ENSP00000354194.3:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTG...
ENST00000653642.1:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA ENSP00000499315.1:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTG...
ENST00000662305.1:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA ENSP00000499226.1:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTG...
ENST00000666778.1:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA ENSP00000499775.1:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTG...
ENST00000667466.1:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA ENSP00000499540.1:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTG...
ENST00000360214.7:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA ENSP00000353344.3:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTG...
ENST00000360938.7:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA ENSP00000354194.3:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTG...
NM_001256295.1:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA NP_001243224.1:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAAT...
NM_005239.5:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA NP_005230.1:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCT...
XM_005260935.1:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA XP_005260992.1:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAAT...
XM_017028290.1:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA XP_016883779.1:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAAT...
NM_005239.6:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA MANE Select NP_005230.1:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCT...
NM_001256295.2:c.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAATTCTTATTTCAAA NP_001243224.1:n.*671_*672insGAAAAATGAAATAAAACCTCAGATGTCTGAAT...