Canonical Allele Identifier: CA2616109663
Gene: APOA4 HGNC NCBI

Linked Data

gnomAD v4: 11-116822582-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822584del , CM000673.2:g.116822584del GRCh38
NC_000011.9:g.116693300del , CM000673.1:g.116693300del GRCh37
NC_000011.8:g.116198510del NCBI36
NG_012044.1:g.5713del

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.176+76del MANE Select ENSP00000350425.3:n.176+76del
ENST00000357780.4:c.176+76del ENSP00000350425.3:n.176+76del
NM_000482.3:c.176+76del NP_000473.2:n.176+76del
NM_000482.4:c.176+76del MANE Select NP_000473.2:n.176+76del
Search 100 bp 5'
Search 100 bp 3'