Canonical Allele Identifier: CA2325105530
Gene: CYP4F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897424_15897437delinsTGTCCCCAAAACCA , CM000681.2:g.15897424_15897437delinsTGTCCCCAAAACCA GRCh38
NC_000019.9:g.16008234_16008247delinsTGTCCCCAAAACCA , CM000681.1:g.16008234_16008247delinsTGTCCCCAAAACCA GRCh37
NC_000019.8:g.15869234_15869247delinsTGTCCCCAAAACCA NCBI36
NG_007971.2:g.5638_5651delinsTGGTTTTGGGGACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.175_188delinsTGGTTTTGGGGACA MANE Select ENSP00000221700.3:p.Trp59=
ENST00000011989.11:c.175_188delinsTGGTTTTGGGGACA ENSP00000011989.8:p.Trp59=
ENST00000221700.10:c.175_188delinsTGGTTTTGGGGACA ENSP00000221700.3:p.Trp59=
ENST00000392846.7:n.49+589_49+602delinsTGGTTTTGGGGACA
ENST00000586927.2:c.175_188delinsTGGTTTTGGGGACA ENSP00000465514.1:p.Trp59=
ENST00000587671.2:c.175_188delinsTGGTTTTGGGGACA ENSP00000467443.2:p.Trp59=
ENST00000608168.1:n.228_241delinsTGGTTTTGGGGACA
NM_001082.4:c.175_188delinsTGGTTTTGGGGACA NP_001073.3:p.Trp59=
NM_001082.5:c.175_188delinsTGGTTTTGGGGACA MANE Select NP_001073.3:p.Trp59=
Search 100 bp 5'
Search 100 bp 3'