Canonical Allele Identifier: CA1519920473
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199074_186199077delinsTACC , CM000666.2:g.186199074_186199077delinsTACC GRCh38
NC_000004.11:g.187120228_187120231delinsTACC , CM000666.1:g.187120228_187120231delinsTACC GRCh37
NC_000004.10:g.187357222_187357225delinsTACC NCBI36
NG_007965.1:g.12555_12558delinsTACC

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.792_795delinsTACC MANE Select ENSP00000368079.4:p.Phe264=
ENST00000378802.4:c.792_795delinsTACC ENSP00000368079.4:p.Phe264=
ENST00000507209.5:n.1633_1636delinsTACC
NM_207352.3:c.792_795delinsTACC NP_997235.3:p.Phe264=
XM_005262935.2:c.792_795delinsTACC XP_005262992.1:p.Phe264=
XM_006714184.2:c.396_399delinsTACC XP_006714247.1:p.Phe132=
XM_005262935.4:c.792_795delinsTACC XP_005262992.1:p.Phe264=
XM_017008037.1:c.396_399delinsTACC XP_016863526.1:p.Phe132=
NM_207352.4:c.792_795delinsTACC MANE Select NP_997235.3:p.Phe264=