Canonical Allele Identifier: CA2325097021

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879565_15879566delinsGC , CM000681.2:g.15879565_15879566delinsGC	GRCh38
NC_000019.9:g.15990375_15990376delinsGC , CM000681.1:g.15990375_15990376delinsGC	GRCh37
NC_000019.8:g.15851375_15851376delinsGC	NCBI36
NG_007971.2:g.23509_23510delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1314+38_1314+39delinsGC MANE Select	ENSP00000221700.3:n.1314+38_1314+39delinsGC
ENST00000011989.11:c.1314+38_1314+39delinsGC	ENSP00000011989.8:n.1314+38_1314+39delinsGC
ENST00000221700.10:c.1314+38_1314+39delinsGC	ENSP00000221700.3:n.1314+38_1314+39delinsGC
ENST00000392846.7:n.1257+38_1257+39delinsGC
ENST00000589654.2:c.103-138_103-137delinsGC
NM_001082.4:c.1314+38_1314+39delinsGC	NP_001073.3:n.1314+38_1314+39delinsGC
NM_001082.5:c.1314+38_1314+39delinsGC MANE Select	NP_001073.3:n.1314+38_1314+39delinsGC