Canonical Allele Identifier: CA8678510
Gene: TRIM37 HGNC NCBI

Linked Data

ClinVar Variation Id: 324207
dbSNP Id: rs367700401

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.59064418del , CM000679.2:g.59064418del GRCh38
NC_000017.10:g.57141779del , CM000679.1:g.57141779del GRCh37
NC_000017.9:g.54496561del NCBI36
NG_009298.1:g.47498del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262294.12:c.810-3del MANE Select ENSP00000262294.7:n.810-3del
ENST00000262294.11:c.810-3del ENSP00000262294.7:n.810-3del
ENST00000393065.6:c.708-3del ENSP00000376784.2:n.708-3del
ENST00000393066.7:c.810-3del ENSP00000376785.3:n.810-3del
ENST00000577554.5:c.*682-3del ENSP00000462340.1:n.*682-3del
ENST00000581468.1:c.432-3del ENSP00000462863.1:n.432-3del
ENST00000582852.1:n.248-3del
NM_001005207.2:c.810-3del NP_001005207.1:n.810-3del
NM_015294.3:c.810-3del NP_056109.1:n.810-3del
XM_005257385.1:c.810-3del XP_005257442.1:n.810-3del
XM_005257387.1:c.708-3del XP_005257444.1:n.708-3del
XM_005257389.1:c.810-3del XP_005257446.1:n.810-3del
XM_005257390.1:c.810-3del XP_005257447.1:n.810-3del
XM_011524831.1:c.810-3del XP_011523133.1:n.810-3del
XM_011524832.1:c.810-3del XP_011523134.1:n.810-3del
XM_011524833.1:c.810-1760del XP_011523135.1:n.810-1760del
XM_011524834.1:c.708-3del XP_011523136.1:n.708-3del
XM_011524835.1:c.810-3del XP_011523137.1:n.810-3del
XM_011524836.1:c.810-3del XP_011523138.1:n.810-3del
XM_011524837.1:c.810-3del XP_011523139.1:n.810-3del
NM_001005207.4:c.810-3del NP_001005207.1:n.810-3del
NM_001320987.2:c.708-3del NP_001307916.1:n.708-3del
NM_001320988.2:c.810-3del NP_001307917.1:n.810-3del
NM_001320989.2:c.810-3del NP_001307918.1:n.810-3del
NM_001320990.2:c.444-3del NP_001307919.1:n.444-3del
NM_001353082.1:c.708-3del NP_001340011.1:n.708-3del
NM_001353083.1:c.75-3del NP_001340012.1:n.75-3del
NM_001353084.1:c.810-3del NP_001340013.1:n.810-3del
NM_001353085.1:c.348-3del NP_001340014.1:n.348-3del
NM_001353086.1:c.810-1760del NP_001340015.1:n.810-1760del
NM_015294.5:c.810-3del NP_056109.1:n.810-3del
NR_148346.1:n.1313-3del
NR_148347.1:n.1211-3del
XM_011524832.2:c.810-3del XP_011523134.1:n.810-3del
XM_017024662.1:c.810-3del XP_016880151.1:n.810-3del
XM_017024663.2:c.810-3del XP_016880152.1:n.810-3del
XM_017024664.1:c.810-1760del XP_016880153.1:n.810-1760del
XM_017024665.1:c.708-3del XP_016880154.1:n.708-3del
XM_017024667.1:c.810-1760del XP_016880156.1:n.810-1760del
XM_017024669.2:c.708-1760del XP_016880158.1:n.708-1760del
XM_017024670.2:c.708-3del XP_016880159.1:n.708-3del
XM_017024671.2:c.348-3del XP_016880160.1:n.348-3del
XM_017024672.1:c.348-3del XP_016880161.1:n.348-3del
XM_017024673.2:c.75-3del XP_016880162.1:n.75-3del
XM_024450765.1:c.348-3del XP_024306533.1:n.348-3del
NM_015294.6:c.810-3del MANE Select NP_056109.1:n.810-3del
NM_001005207.5:c.810-3del NP_001005207.1:n.810-3del
NM_001320987.3:c.708-3del NP_001307916.1:n.708-3del
NM_001320988.3:c.810-3del NP_001307917.1:n.810-3del
NM_001320989.3:c.810-3del NP_001307918.1:n.810-3del
NM_001320990.3:c.444-3del NP_001307919.1:n.444-3del
NM_001353082.2:c.708-3del NP_001340011.1:n.708-3del
NM_001353083.2:c.75-3del NP_001340012.1:n.75-3del
NM_001353084.2:c.810-3del NP_001340013.1:n.810-3del
NM_001353085.2:c.348-3del NP_001340014.1:n.348-3del
NM_001353086.2:c.810-1760del NP_001340015.1:n.810-1760del
NR_148346.2:n.1229-3del
NR_148347.2:n.1127-3del