Canonical Allele Identifier: CA2325097007

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879549_15879550delinsGC , CM000681.2:g.15879549_15879550delinsGC	GRCh38
NC_000019.9:g.15990359_15990360delinsGC , CM000681.1:g.15990359_15990360delinsGC	GRCh37
NC_000019.8:g.15851359_15851360delinsGC	NCBI36
NG_007971.2:g.23525_23526delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1314+54_1314+55delinsGC MANE Select	ENSP00000221700.3:n.1314+54_1314+55delinsGC
ENST00000011989.11:c.1314+54_1314+55delinsGC	ENSP00000011989.8:n.1314+54_1314+55delinsGC
ENST00000221700.10:c.1314+54_1314+55delinsGC	ENSP00000221700.3:n.1314+54_1314+55delinsGC
ENST00000392846.7:n.1257+54_1257+55delinsGC
ENST00000589654.2:c.103-122_103-121delinsGC
NM_001082.4:c.1314+54_1314+55delinsGC	NP_001073.3:n.1314+54_1314+55delinsGC
NM_001082.5:c.1314+54_1314+55delinsGC MANE Select	NP_001073.3:n.1314+54_1314+55delinsGC