Canonical Allele Identifier: CA2325105725
Gene: CYP4F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897771_15897772delinsGC , CM000681.2:g.15897771_15897772delinsGC GRCh38
NC_000019.9:g.16008581_16008582delinsGC , CM000681.1:g.16008581_16008582delinsGC GRCh37
NC_000019.8:g.15869581_15869582delinsGC NCBI36
NG_007971.2:g.5303_5304delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.-1-160_-1-159delinsGC MANE Select ENSP00000221700.3:n.-1-160_-1-159delinsGC
ENST00000011989.11:c.-1-160_-1-159delinsGC ENSP00000011989.8:n.-1-160_-1-159delinsGC
ENST00000221700.10:c.-1-160_-1-159delinsGC ENSP00000221700.3:n.-1-160_-1-159delinsGC
ENST00000392846.7:n.49+254_49+255delinsGC
ENST00000587671.2:c.-1-160_-1-159delinsGC ENSP00000467443.2:n.-1-160_-1-159delinsGC
ENST00000608168.1:n.53-160_53-159delinsGC
NM_001082.4:c.-1-160_-1-159delinsGC NP_001073.3:n.-1-160_-1-159delinsGC
NM_001082.5:c.-1-160_-1-159delinsGC MANE Select NP_001073.3:n.-1-160_-1-159delinsGC