Canonical Allele Identifier: CA2583147411
Gene: CYP4F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897322_15897323del , CM000681.2:g.15897322_15897323del GRCh38
NC_000019.9:g.16008132_16008133del , CM000681.1:g.16008132_16008133del GRCh37
NC_000019.8:g.15869132_15869133del NCBI36
NG_007971.2:g.5752_5753del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.198+91_198+92del MANE Select ENSP00000221700.3:n.198+91_198+92del
ENST00000011989.11:c.198+91_198+92del ENSP00000011989.8:n.198+91_198+92del
ENST00000221700.10:c.198+91_198+92del ENSP00000221700.3:n.198+91_198+92del
ENST00000392846.7:n.49+703_49+704del
ENST00000586927.2:c.198+91_198+92del ENSP00000465514.1:n.198+91_198+92del
ENST00000587671.2:c.198+91_198+92del ENSP00000467443.2:n.198+91_198+92del
ENST00000608168.1:n.251+91_251+92del
NM_001082.4:c.198+91_198+92del NP_001073.3:n.198+91_198+92del
NM_001082.5:c.198+91_198+92del MANE Select NP_001073.3:n.198+91_198+92del