Canonical Allele Identifier: CA2583145345

Gene: CYP4F2

Linked Data

• gnomAD v4: 19-15879205-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879209del , CM000681.2:g.15879209del	GRCh38
NC_000019.9:g.15990019del , CM000681.1:g.15990019del	GRCh37
NC_000019.8:g.15851019del	NCBI36
NG_007971.2:g.23869del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1397+140del MANE Select	ENSP00000221700.3:n.1397+140del
ENST00000011989.11:c.1397+140del	ENSP00000011989.8:n.1397+140del
ENST00000221700.10:c.1397+140del	ENSP00000221700.3:n.1397+140del
ENST00000392846.7:n.1340+140del
ENST00000589654.2:c.185+140del
NM_001082.4:c.1397+140del	NP_001073.3:n.1397+140del
NM_001082.5:c.1397+140del MANE Select	NP_001073.3:n.1397+140del