Canonical Allele Identifier: CA2830537789
Gene: TRIM60 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.165040654_165040655insAAAACAATCTTATTTGCTCAAACT , CM000666.2:g.165040654_165040655insAAAACAATCTTATTTGCTCAAACT GRCh38
NC_000004.11:g.165961806_165961807insAAAACAATCTTATTTGCTCAAACT , CM000666.1:g.165961806_165961807insAAAACAATCTTATTTGCTCAAACT GRCh37
NC_000004.10:g.166181256_166181257insAAAACAATCTTATTTGCTCAAACT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000512596.6:c.582_583insAAAACAATCTTATTTGCTCAAACT MANE Select ENSP00000421142.1:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr
ENST00000647760.1:c.582_583insAAAACAATCTTATTTGCTCAAACT ENSP00000497401.1:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr
ENST00000341062.6:c.582_583insAAAACAATCTTATTTGCTCAAACT ENSP00000343765.5:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr
ENST00000508504.1:c.582_583insAAAACAATCTTATTTGCTCAAACT ENSP00000426496.1:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr
ENST00000512596.5:c.582_583insAAAACAATCTTATTTGCTCAAACT ENSP00000421142.1:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr
NM_001258025.1:c.582_583insAAAACAATCTTATTTGCTCAAACT NP_001244954.1:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr
NM_152620.2:c.582_583insAAAACAATCTTATTTGCTCAAACT NP_689833.1:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr
XM_011531681.1:c.582_583insAAAACAATCTTATTTGCTCAAACT XP_011529983.1:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr
XM_011531682.1:c.582_583insAAAACAATCTTATTTGCTCAAACT XP_011529984.1:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr
XM_011531683.1:c.582_583insAAAACAATCTTATTTGCTCAAACT XP_011529985.1:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr
XM_011531683.2:c.582_583insAAAACAATCTTATTTGCTCAAACT XP_011529985.1:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr
NM_152620.3:c.582_583insAAAACAATCTTATTTGCTCAAACT MANE Select NP_689833.1:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr
NM_001258025.2:c.582_583insAAAACAATCTTATTTGCTCAAACT NP_001244954.1:p.Leu194_Gln195insLysThrIleLeuPheAlaGlnThr