Canonical Allele Identifier: CA2583147560
Gene: CYP4F2 HGNC NCBI

Linked Data

gnomAD v4: 19-15897440-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897442del , CM000681.2:g.15897442del GRCh38
NC_000019.9:g.16008252del , CM000681.1:g.16008252del GRCh37
NC_000019.8:g.15869252del NCBI36
NG_007971.2:g.5634del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.171del MANE Select ENSP00000221700.3:p.Asn58ThrfsTer17
ENST00000011989.11:c.171del ENSP00000011989.8:p.Asn58ThrfsTer9
ENST00000221700.10:c.171del ENSP00000221700.3:p.Asn58ThrfsTer17
ENST00000392846.7:n.49+585del
ENST00000586927.2:c.171del ENSP00000465514.1:p.Asn58ThrfsTer17
ENST00000587671.2:c.171del ENSP00000467443.2:p.Asn58ThrfsTer?
ENST00000608168.1:n.224del
NM_001082.4:c.171del NP_001073.3:p.Asn58ThrfsTer17
NM_001082.5:c.171del MANE Select NP_001073.3:p.Asn58ThrfsTer17
Search 100 bp 5'
Search 100 bp 3'