Canonical Allele Identifier: CA783688006

Gene: CYP4F2

Linked Data

• dbSNP Id: rs1304109965
• MyVariant Identifiers: chr19:g.16008111del (hg19) ; chr19:g.15897301del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897302del , CM000681.2:g.15897302del	GRCh38
NC_000019.9:g.16008112del , CM000681.1:g.16008112del	GRCh37
NC_000019.8:g.15869112del	NCBI36
NG_007971.2:g.5774del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.198+113del MANE Select	ENSP00000221700.3:n.198+113del
ENST00000011989.11:c.198+113del	ENSP00000011989.8:n.198+113del
ENST00000221700.10:c.198+113del	ENSP00000221700.3:n.198+113del
ENST00000392846.7:n.49+725del
ENST00000586927.2:c.198+113del	ENSP00000465514.1:n.198+113del
ENST00000587671.2:c.198+113del	ENSP00000467443.2:n.198+113del
ENST00000608168.1:n.251+113del
NM_001082.4:c.198+113del	NP_001073.3:n.198+113del
NM_001082.5:c.198+113del MANE Select	NP_001073.3:n.198+113del