Canonical Allele Identifier: CA2583147484

Gene: CYP4F2

Linked Data

• gnomAD v4: 19-15897341-ACTCCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897342_15897346del , CM000681.2:g.15897342_15897346del	GRCh38
NC_000019.9:g.16008152_16008156del , CM000681.1:g.16008152_16008156del	GRCh37
NC_000019.8:g.15869152_15869156del	NCBI36
NG_007971.2:g.5729_5733del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.198+68_198+72del MANE Select	ENSP00000221700.3:n.198+68_198+72del
ENST00000011989.11:c.198+68_198+72del	ENSP00000011989.8:n.198+68_198+72del
ENST00000221700.10:c.198+68_198+72del	ENSP00000221700.3:n.198+68_198+72del
ENST00000392846.7:n.49+680_49+684del
ENST00000586927.2:c.198+68_198+72del	ENSP00000465514.1:n.198+68_198+72del
ENST00000587671.2:c.198+68_198+72del	ENSP00000467443.2:n.198+68_198+72del
ENST00000608168.1:n.251+68_251+72del
NM_001082.4:c.198+68_198+72del	NP_001073.3:n.198+68_198+72del
NM_001082.5:c.198+68_198+72del MANE Select	NP_001073.3:n.198+68_198+72del