Canonical Allele Identifier: CA2201204862

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.681776T= , CM000678.2:g.681776T= GRCh38
NC_000016.9:g.731776T= , CM000678.1:g.731776T= GRCh37
NC_000016.8:g.671777T= NCBI36
NG_034141.1:g.6666T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000219548.9:c.525-17T= (STUB1) MANE Select ENSP00000219548.4:n.525-17T=
ENST00000609261.6:c.*1018A= (JMJD8) MANE Select ENSP00000477481.1:n.*1018A=
ENST00000219548.8:c.525-17T= (STUB1) ENSP00000219548.4:n.525-17T=
ENST00000412368.6:c.*1018A= (JMJD8) ENSP00000399475.2:n.*1018A=
ENST00000563505.5:n.621-17T= (STUB1)
ENST00000564316.1:c.124-17T= (STUB1)
ENST00000564370.5:c.309-17T= (STUB1) ENSP00000456875.1:n.309-17T=
ENST00000565302.5:n.1897A= (JMJD8)
ENST00000565677.5:c.309-17T= (STUB1) ENSP00000457228.1:n.309-17T=
ENST00000566181.2:n.294-17T= (STUB1)
ENST00000566408.5:c.242-17T= (STUB1)
ENST00000567120.5:n.2100A= (JMJD8)
ENST00000567173.5:c.468-17T= (STUB1) ENSP00000456591.1:n.468-17T=
ENST00000568689.5:n.1921A= (JMJD8)
ENST00000569248.5:n.1099-17T= (STUB1)
ENST00000609261.5:c.*1018A= (JMJD8) ENSP00000477481.1:n.*1018A=
ENST00000620831.4:c.-50+38473T= (MSLN) ENSP00000482893.1:n.-50+38473T=
NM_001005920.2:c.*1018A= (JMJD8) NP_001005920.2:n.*1018A=
NM_001293197.1:c.309-17T= (STUB1) NP_001280126.1:n.309-17T=
NM_005861.3:c.525-17T= (STUB1) NP_005852.2:n.525-17T=
XM_005255295.3:c.*1052A= (JMJD8) XP_005255352.1:n.*1052A=
XM_005255297.3:c.*1018A= (JMJD8) XP_005255354.1:n.*1018A=
XM_011522474.1:c.*1018A= (JMJD8) XP_011520776.1:n.*1018A=
NM_001005920.3:c.*1018A= (JMJD8) NP_001005920.3:n.*1018A=
NM_001323918.2:c.*1052A= (JMJD8) NP_001310847.2:n.*1052A=
NM_001323919.2:c.*1018A= (JMJD8) NP_001310848.2:n.*1018A=
NM_001323920.2:c.*1018A= (JMJD8) NP_001310849.2:n.*1018A=
NM_001323922.2:c.*1052A= (JMJD8) NP_001310851.2:n.*1052A=
NR_136650.2:n.1911A= (JMJD8)
NR_136651.2:n.1916A= (JMJD8)
NR_136652.2:n.1826A= (JMJD8)
NM_001005920.4:c.*1018A= (JMJD8) MANE Select NP_001005920.3:n.*1018A=
NM_005861.4:c.525-17T= (STUB1) MANE Select NP_005852.2:n.525-17T=
NM_001293197.2:c.309-17T= (STUB1) NP_001280126.1:n.309-17T=
NM_001323918.3:c.*1052A= (JMJD8) NP_001310847.2:n.*1052A=
NM_001323919.3:c.*1018A= (JMJD8) NP_001310848.2:n.*1018A=
NM_001323920.3:c.*1018A= (JMJD8) NP_001310849.2:n.*1018A=
NM_001323922.3:c.*1052A= (JMJD8) NP_001310851.2:n.*1052A=
NR_136650.3:n.1911A= (JMJD8)
NR_136651.3:n.1916A= (JMJD8)
NR_136652.3:n.1826A= (JMJD8)