Canonical Allele Identifier: CA2324977485

Gene: CYP4F3

Linked Data

• dbSNP Id: rs1972445546
• gnomAD v4: 19-15640955-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640960del , CM000681.2:g.15640960del	GRCh38
NC_000019.9:g.15751770del , CM000681.1:g.15751770del	GRCh37
NC_000019.8:g.15612770del	NCBI36
NG_007964.1:g.5064del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221307.13:c.-2+15del MANE Select	ENSP00000221307.6:n.-2+15del
ENST00000221307.12:c.-2+15del	ENSP00000221307.6:n.-2+15del
ENST00000586182.6:c.-2+31del	ENSP00000466395.1:n.-2+31del
ENST00000591058.5:c.-2+15del	ENSP00000466988.1:n.-2+15del
ENST00000592279.6:n.49+15del
ENST00000620621.4:c.344-6092del	ENSP00000478605.1:n.344-6092del
NM_000896.2:c.-2+15del	NP_000887.2:n.-2+15del
NM_001199208.1:c.-2+15del	NP_001186137.1:n.-2+15del
NM_001199209.1:c.-2+31del	NP_001186138.1:n.-2+31del
NM_000896.3:c.-2+15del MANE Select	NP_000887.2:n.-2+15del
NM_001199208.2:c.-2+15del	NP_001186137.1:n.-2+15del
NM_001199209.2:c.-2+31del	NP_001186138.1:n.-2+31del