Canonical Allele Identifier: CA2583147654

Gene: CYP4F2

Linked Data

• gnomAD v4: 19-15897735-T-TGGGTAAAAAGGGGCTGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897736_15897753dup , CM000681.2:g.15897736_15897753dup	GRCh38
NC_000019.9:g.16008546_16008563dup , CM000681.1:g.16008546_16008563dup	GRCh37
NC_000019.8:g.15869546_15869563dup	NCBI36
NG_007971.2:g.5322_5339dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.-1-141_-1-124dup MANE Select	ENSP00000221700.3:n.-1-141_-1-124dup
ENST00000011989.11:c.-1-141_-1-124dup	ENSP00000011989.8:n.-1-141_-1-124dup
ENST00000221700.10:c.-1-141_-1-124dup	ENSP00000221700.3:n.-1-141_-1-124dup
ENST00000392846.7:n.49+273_49+290dup
ENST00000587671.2:c.-1-141_-1-124dup	ENSP00000467443.2:n.-1-141_-1-124dup
ENST00000608168.1:n.53-141_53-124dup
NM_001082.4:c.-1-141_-1-124dup	NP_001073.3:n.-1-141_-1-124dup
NM_001082.5:c.-1-141_-1-124dup MANE Select	NP_001073.3:n.-1-141_-1-124dup