Canonical Allele Identifier: CA2325105652

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897647A= , CM000681.2:g.15897647A=	GRCh38
NC_000019.9:g.16008457A= , CM000681.1:g.16008457A=	GRCh37
NC_000019.8:g.15869457A=	NCBI36
NG_007971.2:g.5428T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.-1-35T= MANE Select	ENSP00000221700.3:n.-1-35T=
ENST00000011989.11:c.-1-35T=	ENSP00000011989.8:n.-1-35T=
ENST00000221700.10:c.-1-35T=	ENSP00000221700.3:n.-1-35T=
ENST00000392846.7:n.49+379T=
ENST00000586927.2:c.-36T=	ENSP00000465514.1:n.-36T=
ENST00000587671.2:c.-1-35T=	ENSP00000467443.2:n.-1-35T=
ENST00000608168.1:n.53-35T=
NM_001082.4:c.-1-35T=	NP_001073.3:n.-1-35T=
NM_001082.5:c.-1-35T= MANE Select	NP_001073.3:n.-1-35T=