Canonical Allele Identifier: CA2520224962

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15889227_15889228insT , CM000681.2:g.15889227_15889228insT	GRCh38
NC_000019.9:g.16000037_16000038insT , CM000681.1:g.16000037_16000038insT	GRCh37
NC_000019.8:g.15861037_15861038insT	NCBI36
NG_007971.2:g.13847_13848insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.918+195_918+196insA MANE Select	ENSP00000221700.3:n.918+195_918+196insA
ENST00000011989.11:c.918+195_918+196insA	ENSP00000011989.8:n.918+195_918+196insA
ENST00000221700.10:c.918+195_918+196insA	ENSP00000221700.3:n.918+195_918+196insA
ENST00000392846.7:n.861+195_861+196insA
ENST00000587671.2:c.*503+195_*503+196insA	ENSP00000467443.2:n.*503+195_*503+196insA
NM_001082.4:c.918+195_918+196insA	NP_001073.3:n.918+195_918+196insA
NM_001082.5:c.918+195_918+196insA MANE Select	NP_001073.3:n.918+195_918+196insA