Canonical Allele Identifier: CA631961371

Gene: CYP4F3

Linked Data

• dbSNP Id: rs1287420703
• gnomAD v2: 19-15751709-A-AAGAAGG
• gnomAD v3: 19-15640899-A-AAGAAGG
• gnomAD v4: 19-15640899-A-AAGAAGG
• MyVariant Identifiers: chr19:g.15751709_15751710insAGAAGG (hg19) ; chr19:g.15640899_15640900insAGAAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640900_15640905dup , CM000681.2:g.15640900_15640905dup	GRCh38
NC_000019.9:g.15751710_15751715dup , CM000681.1:g.15751710_15751715dup	GRCh37
NC_000019.8:g.15612710_15612715dup	NCBI36
NG_007964.1:g.5004_5009dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221307.13:c.-47_-42dup MANE Select	ENSP00000221307.6:n.-47_-42dup
ENST00000221307.12:c.-47_-42dup	ENSP00000221307.6:n.-47_-42dup
ENST00000586182.6:c.-31_-26dup	ENSP00000466395.1:n.-31_-26dup
ENST00000591058.5:c.-47_-42dup	ENSP00000466988.1:n.-47_-42dup
ENST00000592279.6:n.4_9dup
ENST00000620621.4:c.344-6152_344-6147dup	ENSP00000478605.1:n.344-6152_344-6147dup
NM_000896.2:c.-47_-42dup	NP_000887.2:n.-47_-42dup
NM_001199208.1:c.-47_-42dup	NP_001186137.1:n.-47_-42dup
NM_001199209.1:c.-31_-26dup	NP_001186138.1:n.-31_-26dup
NM_000896.3:c.-47_-42dup MANE Select	NP_000887.2:n.-47_-42dup
NM_001199208.2:c.-47_-42dup	NP_001186137.1:n.-47_-42dup
NM_001199209.2:c.-31_-26dup	NP_001186138.1:n.-31_-26dup