Canonical Allele Identifier: CA2813750770

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897336_15897337insACCCAAAA , CM000681.2:g.15897336_15897337insACCCAAAA	GRCh38
NC_000019.9:g.16008146_16008147insACCCAAAA , CM000681.1:g.16008146_16008147insACCCAAAA	GRCh37
NC_000019.8:g.15869146_15869147insACCCAAAA	NCBI36
NG_007971.2:g.5738_5739insTTTTGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.198+77_198+78insTTTTGGGT MANE Select	ENSP00000221700.3:n.198+77_198+78insTTTTGGGT
ENST00000011989.11:c.198+77_198+78insTTTTGGGT	ENSP00000011989.8:n.198+77_198+78insTTTTGGGT
ENST00000221700.10:c.198+77_198+78insTTTTGGGT	ENSP00000221700.3:n.198+77_198+78insTTTTGGGT
ENST00000392846.7:n.49+689_49+690insTTTTGGGT
ENST00000586927.2:c.198+77_198+78insTTTTGGGT	ENSP00000465514.1:n.198+77_198+78insTTTTGGGT
ENST00000587671.2:c.198+77_198+78insTTTTGGGT	ENSP00000467443.2:n.198+77_198+78insTTTTGGGT
ENST00000608168.1:n.251+77_251+78insTTTTGGGT
NM_001082.4:c.198+77_198+78insTTTTGGGT	NP_001073.3:n.198+77_198+78insTTTTGGGT
NM_001082.5:c.198+77_198+78insTTTTGGGT MANE Select	NP_001073.3:n.198+77_198+78insTTTTGGGT