Canonical Allele Identifier: CA2325096868

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879262_15879263delinsAC , CM000681.2:g.15879262_15879263delinsAC	GRCh38
NC_000019.9:g.15990072_15990073delinsAC , CM000681.1:g.15990072_15990073delinsAC	GRCh37
NC_000019.8:g.15851072_15851073delinsAC	NCBI36
NG_007971.2:g.23812_23813delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1397+83_1397+84delinsGT MANE Select	ENSP00000221700.3:n.1397+83_1397+84delinsGT
ENST00000011989.11:c.1397+83_1397+84delinsGT	ENSP00000011989.8:n.1397+83_1397+84delinsGT
ENST00000221700.10:c.1397+83_1397+84delinsGT	ENSP00000221700.3:n.1397+83_1397+84delinsGT
ENST00000392846.7:n.1340+83_1340+84delinsGT
ENST00000589654.2:c.185+83_185+84delinsGT
NM_001082.4:c.1397+83_1397+84delinsGT	NP_001073.3:n.1397+83_1397+84delinsGT
NM_001082.5:c.1397+83_1397+84delinsGT MANE Select	NP_001073.3:n.1397+83_1397+84delinsGT