Canonical Allele Identifier: CA2583145472

Gene: CYP4F2

Linked Data

• gnomAD v4: 19-15879530-T-TCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15879530_15879531insCCA , CM000681.2:g.15879530_15879531insCCA	GRCh38
NC_000019.9:g.15990340_15990341insCCA , CM000681.1:g.15990340_15990341insCCA	GRCh37
NC_000019.8:g.15851340_15851341insCCA	NCBI36
NG_007971.2:g.23544_23545insTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000221700.11:c.1314+73_1314+74insTGG MANE Select	ENSP00000221700.3:n.1314+73_1314+74insTGG...
ENST00000011989.11:c.1314+73_1314+74insTGG	ENSP00000011989.8:n.1314+73_1314+74insTGG...
ENST00000221700.10:c.1314+73_1314+74insTGG	ENSP00000221700.3:n.1314+73_1314+74insTGG...
ENST00000392846.7:n.1257+73_1257+74insTGG
ENST00000589654.2:c.103-103_103-102insTGG
NM_001082.4:c.1314+73_1314+74insTGG	NP_001073.3:n.1314+73_1314+74insTGG
NM_001082.5:c.1314+73_1314+74insTGG MANE Select	NP_001073.3:n.1314+73_1314+74insTGG