Canonical Allele Identifier: CA2583147438

Gene: CYP4F2

Linked Data

• gnomAD v4: 19-15897328-CCCCTTCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897332_15897338del , CM000681.2:g.15897332_15897338del	GRCh38
NC_000019.9:g.16008142_16008148del , CM000681.1:g.16008142_16008148del	GRCh37
NC_000019.8:g.15869142_15869148del	NCBI36
NG_007971.2:g.5740_5746del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.198+79_198+85del MANE Select	ENSP00000221700.3:n.198+79_198+85del
ENST00000011989.11:c.198+79_198+85del	ENSP00000011989.8:n.198+79_198+85del
ENST00000221700.10:c.198+79_198+85del	ENSP00000221700.3:n.198+79_198+85del
ENST00000392846.7:n.49+691_49+697del
ENST00000586927.2:c.198+79_198+85del	ENSP00000465514.1:n.198+79_198+85del
ENST00000587671.2:c.198+79_198+85del	ENSP00000467443.2:n.198+79_198+85del
ENST00000608168.1:n.251+79_251+85del
NM_001082.4:c.198+79_198+85del	NP_001073.3:n.198+79_198+85del
NM_001082.5:c.198+79_198+85del MANE Select	NP_001073.3:n.198+79_198+85del