Canonical Allele Identifier: CA1519915083
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194555G= , CM000666.2:g.186194555G= GRCh38
NC_000004.11:g.187115709G= , CM000666.1:g.187115709G= GRCh37
NC_000004.10:g.187352703G= NCBI36
NG_007965.1:g.8036G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.270G= MANE Select ENSP00000368079.4:p.Leu90=
ENST00000378802.4:c.270G= ENSP00000368079.4:p.Leu90=
NM_207352.3:c.270G= NP_997235.3:p.Leu90=
XM_005262935.2:c.270G= XP_005262992.1:p.Leu90=
XM_006714184.2:c.-41G= XP_006714247.1:n.-41G=
XM_005262935.4:c.270G= XP_005262992.1:p.Leu90=
XM_017008037.1:c.-41G= XP_016863526.1:n.-41G=
NM_207352.4:c.270G= MANE Select NP_997235.3:p.Leu90=