Canonical Allele Identifier: CA2325097029

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879584_15879586delinsCAG , CM000681.2:g.15879584_15879586delinsCAG	GRCh38
NC_000019.9:g.15990394_15990396delinsCAG , CM000681.1:g.15990394_15990396delinsCAG	GRCh37
NC_000019.8:g.15851394_15851396delinsCAG	NCBI36
NG_007971.2:g.23489_23491delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1314+18_1314+20delinsCTG MANE Select	ENSP00000221700.3:n.1314+18_1314+20delinsCTG
ENST00000011989.11:c.1314+18_1314+20delinsCTG	ENSP00000011989.8:n.1314+18_1314+20delinsCTG
ENST00000221700.10:c.1314+18_1314+20delinsCTG	ENSP00000221700.3:n.1314+18_1314+20delinsCTG
ENST00000392846.7:n.1257+18_1257+20delinsCTG
ENST00000589654.2:c.103-158_103-156delinsCTG
NM_001082.4:c.1314+18_1314+20delinsCTG	NP_001073.3:n.1314+18_1314+20delinsCTG
NM_001082.5:c.1314+18_1314+20delinsCTG MANE Select	NP_001073.3:n.1314+18_1314+20delinsCTG