Canonical Allele Identifier: CA2325105405

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897158_15897162delinsGCAGA , CM000681.2:g.15897158_15897162delinsGCAGA	GRCh38
NC_000019.9:g.16007968_16007972delinsGCAGA , CM000681.1:g.16007968_16007972delinsGCAGA	GRCh37
NC_000019.8:g.15868968_15868972delinsGCAGA	NCBI36
NG_007971.2:g.5913_5917delinsTCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.198+252_198+256delinsTCTGC MANE Select	ENSP00000221700.3:n.198+252_198+256delinsTCTGC
ENST00000011989.11:c.198+252_198+256delinsTCTGC	ENSP00000011989.8:n.198+252_198+256delinsTCTGC
ENST00000221700.10:c.198+252_198+256delinsTCTGC	ENSP00000221700.3:n.198+252_198+256delinsTCTGC
ENST00000392846.7:n.49+864_49+868delinsTCTGC
ENST00000586927.2:c.198+252_198+256delinsTCTGC	ENSP00000465514.1:n.198+252_198+256delinsTCTGC
ENST00000587671.2:c.198+252_198+256delinsTCTGC	ENSP00000467443.2:n.198+252_198+256delinsTCTGC
ENST00000608168.1:n.251+252_251+256delinsTCTGC
NM_001082.4:c.198+252_198+256delinsTCTGC	NP_001073.3:n.198+252_198+256delinsTCTGC
NM_001082.5:c.198+252_198+256delinsTCTGC MANE Select	NP_001073.3:n.198+252_198+256delinsTCTGC