Canonical Allele Identifier: CA2583147392

Gene: CYP4F2

Linked Data

• gnomAD v4: 19-15897318-T-TTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897318_15897319insTCC , CM000681.2:g.15897318_15897319insTCC	GRCh38
NC_000019.9:g.16008128_16008129insTCC , CM000681.1:g.16008128_16008129insTCC	GRCh37
NC_000019.8:g.15869128_15869129insTCC	NCBI36
NG_007971.2:g.5756_5757insGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.198+95_198+96insGGA MANE Select	ENSP00000221700.3:n.198+95_198+96insGGA
ENST00000011989.11:c.198+95_198+96insGGA	ENSP00000011989.8:n.198+95_198+96insGGA
ENST00000221700.10:c.198+95_198+96insGGA	ENSP00000221700.3:n.198+95_198+96insGGA
ENST00000392846.7:n.49+707_49+708insGGA
ENST00000586927.2:c.198+95_198+96insGGA	ENSP00000465514.1:n.198+95_198+96insGGA
ENST00000587671.2:c.198+95_198+96insGGA	ENSP00000467443.2:n.198+95_198+96insGGA
ENST00000608168.1:n.251+95_251+96insGGA
NM_001082.4:c.198+95_198+96insGGA	NP_001073.3:n.198+95_198+96insGGA
NM_001082.5:c.198+95_198+96insGGA MANE Select	NP_001073.3:n.198+95_198+96insGGA