Canonical Allele Identifier: CA2611124212
Gene: EIF3A HGNC NCBI

Linked Data

gnomAD v4: 10-119050563-CTTT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119050566_119050568del , CM000672.2:g.119050566_119050568del GRCh38
NC_000010.10:g.120810078_120810080del , CM000672.1:g.120810078_120810080del GRCh37
NC_000010.9:g.120800068_120800070del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369144.8:c.2428_2430del MANE Select ENSP00000358140.3:p.Lys810del
ENST00000369144.7:c.2428_2430del ENSP00000358140.3:p.Lys810del
ENST00000541549.2:c.2428_2430del ENSP00000438178.2:p.Lys810del
NM_003750.2:c.2428_2430del NP_003741.1:p.Lys810del
NM_003750.3:c.2428_2430del NP_003741.1:p.Lys810del
NM_003750.4:c.2428_2430del MANE Select NP_003741.1:p.Lys810del
Search 100 bp 5'
Search 100 bp 3'