Canonical Allele Identifier: CA2583147561
Gene: CYP4F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897490_15897494dup , CM000681.2:g.15897490_15897494dup GRCh38
NC_000019.9:g.16008300_16008304dup , CM000681.1:g.16008300_16008304dup GRCh37
NC_000019.8:g.15869300_15869304dup NCBI36
NG_007971.2:g.5581_5585dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.118_122dup MANE Select ENSP00000221700.3:p.Phe41LeufsTer?
ENST00000011989.11:c.118_122dup ENSP00000011989.8:p.Phe41LeufsTer28
ENST00000221700.10:c.118_122dup ENSP00000221700.3:p.Phe41LeufsTer?
ENST00000392846.7:n.49+532_49+536dup
ENST00000586927.2:c.118_122dup ENSP00000465514.1:p.Phe41LeufsTer?
ENST00000587671.2:c.118_122dup ENSP00000467443.2:p.Phe41LeufsTer?
ENST00000608168.1:n.171_175dup
NM_001082.4:c.118_122dup NP_001073.3:p.Phe41LeufsTer?
NM_001082.5:c.118_122dup MANE Select NP_001073.3:p.Phe41LeufsTer?