Canonical Allele Identifier: CA2324977483

Gene: CYP4F3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640955_15640956delinsTG , CM000681.2:g.15640955_15640956delinsTG	GRCh38
NC_000019.9:g.15751765_15751766delinsTG , CM000681.1:g.15751765_15751766delinsTG	GRCh37
NC_000019.8:g.15612765_15612766delinsTG	NCBI36
NG_007964.1:g.5059_5060delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221307.13:c.-2+10_-2+11delinsTG MANE Select	ENSP00000221307.6:n.-2+10_-2+11delinsTG
ENST00000221307.12:c.-2+10_-2+11delinsTG	ENSP00000221307.6:n.-2+10_-2+11delinsTG
ENST00000586182.6:c.-2+26_-2+27delinsTG	ENSP00000466395.1:n.-2+26_-2+27delinsTG
ENST00000591058.5:c.-2+10_-2+11delinsTG	ENSP00000466988.1:n.-2+10_-2+11delinsTG
ENST00000592279.6:n.49+10_49+11delinsTG
ENST00000620621.4:c.344-6097_344-6096delinsTG	ENSP00000478605.1:n.344-6097_344-6096delinsTG
NM_000896.2:c.-2+10_-2+11delinsTG	NP_000887.2:n.-2+10_-2+11delinsTG
NM_001199208.1:c.-2+10_-2+11delinsTG	NP_001186137.1:n.-2+10_-2+11delinsTG
NM_001199209.1:c.-2+26_-2+27delinsTG	NP_001186138.1:n.-2+26_-2+27delinsTG
NM_000896.3:c.-2+10_-2+11delinsTG MANE Select	NP_000887.2:n.-2+10_-2+11delinsTG
NM_001199208.2:c.-2+10_-2+11delinsTG	NP_001186137.1:n.-2+10_-2+11delinsTG
NM_001199209.2:c.-2+26_-2+27delinsTG	NP_001186138.1:n.-2+26_-2+27delinsTG