Canonical Allele Identifier: CA2201204853

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.681772_681773delinsCG , CM000678.2:g.681772_681773delinsCG GRCh38
NC_000016.9:g.731772_731773delinsCG , CM000678.1:g.731772_731773delinsCG GRCh37
NC_000016.8:g.671773_671774delinsCG NCBI36
NG_034141.1:g.6662_6663delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000219548.9:c.525-21_525-20delinsCG (STUB1) MANE Select ENSP00000219548.4:n.525-21_525-20delinsCG
ENST00000609261.6:c.*1021_*1022delinsCG (JMJD8) MANE Select ENSP00000477481.1:n.*1021_*1022delinsCG
ENST00000219548.8:c.525-21_525-20delinsCG (STUB1) ENSP00000219548.4:n.525-21_525-20delinsCG
ENST00000412368.6:c.*1021_*1022delinsCG (JMJD8) ENSP00000399475.2:n.*1021_*1022delinsCG
ENST00000563505.5:n.621-21_621-20delinsCG (STUB1)
ENST00000564316.1:c.124-21_124-20delinsCG (STUB1)
ENST00000564370.5:c.309-21_309-20delinsCG (STUB1) ENSP00000456875.1:n.309-21_309-20delinsCG
ENST00000565302.5:n.1900_1901delinsCG (JMJD8)
ENST00000565677.5:c.309-21_309-20delinsCG (STUB1) ENSP00000457228.1:n.309-21_309-20delinsCG
ENST00000566181.2:n.294-21_294-20delinsCG (STUB1)
ENST00000566408.5:c.242-21_242-20delinsCG (STUB1)
ENST00000567120.5:n.2103_2104delinsCG (JMJD8)
ENST00000567173.5:c.468-21_468-20delinsCG (STUB1) ENSP00000456591.1:n.468-21_468-20delinsCG
ENST00000568689.5:n.1924_1925delinsCG (JMJD8)
ENST00000569248.5:n.1099-21_1099-20delinsCG (STUB1)
ENST00000609261.5:c.*1021_*1022delinsCG (JMJD8) ENSP00000477481.1:n.*1021_*1022delinsCG
ENST00000620831.4:c.-50+38469_-50+38470delinsCG (MSLN) ENSP00000482893.1:n.-50+38469_-50+38470delinsCG
NM_001005920.2:c.*1021_*1022delinsCG (JMJD8) NP_001005920.2:n.*1021_*1022delinsCG
NM_001293197.1:c.309-21_309-20delinsCG (STUB1) NP_001280126.1:n.309-21_309-20delinsCG
NM_005861.3:c.525-21_525-20delinsCG (STUB1) NP_005852.2:n.525-21_525-20delinsCG
XM_005255295.3:c.*1055_*1056delinsCG (JMJD8) XP_005255352.1:n.*1055_*1056delinsCG
XM_005255297.3:c.*1021_*1022delinsCG (JMJD8) XP_005255354.1:n.*1021_*1022delinsCG
XM_011522474.1:c.*1021_*1022delinsCG (JMJD8) XP_011520776.1:n.*1021_*1022delinsCG
NM_001005920.3:c.*1021_*1022delinsCG (JMJD8) NP_001005920.3:n.*1021_*1022delinsCG
NM_001323918.2:c.*1055_*1056delinsCG (JMJD8) NP_001310847.2:n.*1055_*1056delinsCG
NM_001323919.2:c.*1021_*1022delinsCG (JMJD8) NP_001310848.2:n.*1021_*1022delinsCG
NM_001323920.2:c.*1021_*1022delinsCG (JMJD8) NP_001310849.2:n.*1021_*1022delinsCG
NM_001323922.2:c.*1055_*1056delinsCG (JMJD8) NP_001310851.2:n.*1055_*1056delinsCG
NR_136650.2:n.1914_1915delinsCG (JMJD8)
NR_136651.2:n.1919_1920delinsCG (JMJD8)
NR_136652.2:n.1829_1830delinsCG (JMJD8)
NM_001005920.4:c.*1021_*1022delinsCG (JMJD8) MANE Select NP_001005920.3:n.*1021_*1022delinsCG
NM_005861.4:c.525-21_525-20delinsCG (STUB1) MANE Select NP_005852.2:n.525-21_525-20delinsCG
NM_001293197.2:c.309-21_309-20delinsCG (STUB1) NP_001280126.1:n.309-21_309-20delinsCG
NM_001323918.3:c.*1055_*1056delinsCG (JMJD8) NP_001310847.2:n.*1055_*1056delinsCG
NM_001323919.3:c.*1021_*1022delinsCG (JMJD8) NP_001310848.2:n.*1021_*1022delinsCG
NM_001323920.3:c.*1021_*1022delinsCG (JMJD8) NP_001310849.2:n.*1021_*1022delinsCG
NM_001323922.3:c.*1055_*1056delinsCG (JMJD8) NP_001310851.2:n.*1055_*1056delinsCG
NR_136650.3:n.1914_1915delinsCG (JMJD8)
NR_136651.3:n.1919_1920delinsCG (JMJD8)
NR_136652.3:n.1829_1830delinsCG (JMJD8)