Canonical Allele Identifier: CA2325096975
Gene: CYP4F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879487_15879491delinsGAGAC , CM000681.2:g.15879487_15879491delinsGAGAC GRCh38
NC_000019.9:g.15990297_15990301delinsGAGAC , CM000681.1:g.15990297_15990301delinsGAGAC GRCh37
NC_000019.8:g.15851297_15851301delinsGAGAC NCBI36
NG_007971.2:g.23584_23588delinsGTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1315-63_1315-59delinsGTCTC MANE Select ENSP00000221700.3:n.1315-63_1315-59delinsGTCTC
ENST00000011989.11:c.1315-63_1315-59delinsGTCTC ENSP00000011989.8:n.1315-63_1315-59delinsGTCTC
ENST00000221700.10:c.1315-63_1315-59delinsGTCTC ENSP00000221700.3:n.1315-63_1315-59delinsGTCTC
ENST00000392846.7:n.1258-63_1258-59delinsGTCTC
ENST00000589654.2:c.103-63_103-59delinsGTCTC
NM_001082.4:c.1315-63_1315-59delinsGTCTC NP_001073.3:n.1315-63_1315-59delinsGTCTC
NM_001082.5:c.1315-63_1315-59delinsGTCTC MANE Select NP_001073.3:n.1315-63_1315-59delinsGTCTC