Canonical Allele Identifier: CA3035639
Gene: AIMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 590774
dbSNP Id: rs750731609

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.106327503del , CM000666.2:g.106327503del GRCh38
NC_000004.11:g.107248660del , CM000666.1:g.107248660del GRCh37
NC_000004.10:g.107468109del NCBI36
NG_028166.1:g.16894del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394701.6:c.-109del ENSP00000378191.5:n.-109del
ENST00000442366.6:c.162del ENSP00000405248.2:p.Lys54AsnfsTer2
ENST00000673381.2:n.1223del
ENST00000683179.1:n.587del
ENST00000684504.1:c.162del ENSP00000507352.1:p.Lys54AsnfsTer2
ENST00000394701.5:c.234del ENSP00000378191.4:p.Lys78AsnfsTer2
ENST00000671868.1:c.162del ENSP00000499850.1:p.Lys54AsnfsTer2
ENST00000671960.1:c.162del ENSP00000500025.1:p.Lys54AsnfsTer2
ENST00000672003.1:c.162del ENSP00000500187.1:p.Lys54AsnfsTer2
ENST00000672285.1:c.162del ENSP00000500668.1:p.Lys54AsnfsTer2
ENST00000672328.1:c.162del ENSP00000500159.1:p.Lys54AsnfsTer2
ENST00000672337.1:c.162del ENSP00000499921.1:p.Lys54AsnfsTer2
ENST00000672341.1:c.162del MANE Select ENSP00000500620.1:p.Lys54AsnfsTer2
ENST00000672911.1:c.162del ENSP00000500170.1:p.Lys54AsnfsTer2
ENST00000673018.1:c.162del ENSP00000500732.1:p.Lys54AsnfsTer2
ENST00000673123.1:c.162del ENSP00000500794.1:p.Lys54AsnfsTer2
ENST00000673381.1:n.1223del
ENST00000358008.7:c.162del ENSP00000350699.3:p.Lys54AsnfsTer2
ENST00000394701.4:c.234del ENSP00000378191.4:p.Lys78AsnfsTer2
ENST00000442366.5:c.162del ENSP00000405248.1:p.Lys54AsnfsTer2
ENST00000510207.5:c.162del ENSP00000423681.1:p.Lys54AsnfsTer2
NM_001142415.1:c.162del NP_001135887.1:p.Lys54AsnfsTer2
NM_001142416.1:c.234del NP_001135888.1:p.Lys78AsnfsTer2
NM_004757.3:c.162del NP_004748.2:p.Lys54AsnfsTer2
XM_017008835.2:c.162del XP_016864324.1:p.Lys54AsnfsTer2
XM_017008836.2:c.162del XP_016864325.1:p.Lys54AsnfsTer2
NM_001142416.2:c.162del MANE Select NP_001135888.2:p.Lys54AsnfsTer2
NM_001142415.2:c.162del NP_001135887.1:p.Lys54AsnfsTer2
NM_004757.4:c.162del NP_004748.2:p.Lys54AsnfsTer2