Canonical Allele Identifier: CA2325101730

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15889201_15889202delinsTA , CM000681.2:g.15889201_15889202delinsTA	GRCh38
NC_000019.9:g.16000011_16000012delinsTA , CM000681.1:g.16000011_16000012delinsTA	GRCh37
NC_000019.8:g.15861011_15861012delinsTA	NCBI36
NG_007971.2:g.13873_13874delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.918+221_918+222delinsTA MANE Select	ENSP00000221700.3:n.918+221_918+222delinsTA
ENST00000011989.11:c.918+221_918+222delinsTA	ENSP00000011989.8:n.918+221_918+222delinsTA
ENST00000221700.10:c.918+221_918+222delinsTA	ENSP00000221700.3:n.918+221_918+222delinsTA
ENST00000392846.7:n.861+221_861+222delinsTA
ENST00000587671.2:c.*503+221_*503+222delinsTA	ENSP00000467443.2:n.*503+221_*503+222delinsTA
NM_001082.4:c.918+221_918+222delinsTA	NP_001073.3:n.918+221_918+222delinsTA
NM_001082.5:c.918+221_918+222delinsTA MANE Select	NP_001073.3:n.918+221_918+222delinsTA