Canonical Allele Identifier: CA2583145342

Gene: CYP4F2

Linked Data

• gnomAD v4: 19-15879204-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879204_15879205insA , CM000681.2:g.15879204_15879205insA	GRCh38
NC_000019.9:g.15990014_15990015insA , CM000681.1:g.15990014_15990015insA	GRCh37
NC_000019.8:g.15851014_15851015insA	NCBI36
NG_007971.2:g.23870_23871insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.1397+141_1397+142insT MANE Select	ENSP00000221700.3:n.1397+141_1397+142insT
ENST00000011989.11:c.1397+141_1397+142insT	ENSP00000011989.8:n.1397+141_1397+142insT
ENST00000221700.10:c.1397+141_1397+142insT	ENSP00000221700.3:n.1397+141_1397+142insT
ENST00000392846.7:n.1340+141_1340+142insT
ENST00000589654.2:c.185+141_185+142insT
NM_001082.4:c.1397+141_1397+142insT	NP_001073.3:n.1397+141_1397+142insT
NM_001082.5:c.1397+141_1397+142insT MANE Select	NP_001073.3:n.1397+141_1397+142insT