Canonical Allele Identifier: CA2741615712

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897487_15897510del , CM000681.2:g.15897487_15897510del	GRCh38
NC_000019.9:g.16008297_16008320del , CM000681.1:g.16008297_16008320del	GRCh37
NC_000019.8:g.15869297_15869320del	NCBI36
NG_007971.2:g.5565_5588del

Transcript Alleles

HGVS	Amino-acid change
ENST00000221700.11:c.102_125del MANE Select	ENSP00000221700.3:p.Leu35_Tyr42del
ENST00000011989.11:c.102_125del	ENSP00000011989.8:p.Leu35_Tyr42del
ENST00000221700.10:c.102_125del	ENSP00000221700.3:p.Leu35_Tyr42del
ENST00000392846.7:n.49+516_49+539del
ENST00000586927.2:c.102_125del	ENSP00000465514.1:p.Leu35_Tyr42del
ENST00000587671.2:c.102_125del	ENSP00000467443.2:p.Leu35_Tyr42del
ENST00000608168.1:n.155_178del
NM_001082.4:c.102_125del	NP_001073.3:p.Leu35_Tyr42del
NM_001082.5:c.102_125del MANE Select	NP_001073.3:p.Leu35_Tyr42del