Canonical Allele Identifier: CA2324977566

Gene: CYP4F3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15641132_15641133delinsCT , CM000681.2:g.15641132_15641133delinsCT	GRCh38
NC_000019.9:g.15751942_15751943delinsCT , CM000681.1:g.15751942_15751943delinsCT	GRCh37
NC_000019.8:g.15612942_15612943delinsCT	NCBI36
NG_007964.1:g.5236_5237delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000221307.13:c.-2+187_-2+188delinsCT MANE Select	ENSP00000221307.6:n.-2+187_-2+188delinsCT...
ENST00000221307.12:c.-2+187_-2+188delinsCT	ENSP00000221307.6:n.-2+187_-2+188delinsCT...
ENST00000586182.6:c.-2+203_-2+204delinsCT	ENSP00000466395.1:n.-2+203_-2+204delinsCT...
ENST00000591058.5:c.-2+187_-2+188delinsCT	ENSP00000466988.1:n.-2+187_-2+188delinsCT...
ENST00000592279.6:n.49+187_49+188delinsCT
ENST00000620621.4:c.344-5920_344-5919delinsCT	ENSP00000478605.1:n.344-5920_344-5919deli...
NM_000896.2:c.-2+187_-2+188delinsCT	NP_000887.2:n.-2+187_-2+188delinsCT
NM_001199208.1:c.-2+187_-2+188delinsCT	NP_001186137.1:n.-2+187_-2+188delinsCT
NM_001199209.1:c.-2+203_-2+204delinsCT	NP_001186138.1:n.-2+203_-2+204delinsCT
NM_000896.3:c.-2+187_-2+188delinsCT MANE Select	NP_000887.2:n.-2+187_-2+188delinsCT
NM_001199208.2:c.-2+187_-2+188delinsCT	NP_001186137.1:n.-2+187_-2+188delinsCT
NM_001199209.2:c.-2+203_-2+204delinsCT	NP_001186138.1:n.-2+203_-2+204delinsCT