Canonical Allele Identifier: CA1519891329
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208964T= , CM000666.2:g.186208964T= GRCh38
NC_000004.11:g.187130118T= , CM000666.1:g.187130118T= GRCh37
NC_000004.10:g.187367112T= NCBI36
NG_007965.1:g.22445T=
NG_012095.2:g.4986T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1190T= MANE Select ENSP00000368079.4:p.Leu397=
ENST00000378802.4:c.1190T= ENSP00000368079.4:p.Leu397=
ENST00000502665.1:n.425T=
ENST00000507209.5:n.5888T=
ENST00000513354.5:n.280T=
NM_207352.3:c.1190T= NP_997235.3:p.Leu397=
XM_005262935.2:c.1190T= XP_005262992.1:p.Leu397=
XM_006714184.2:c.794T= XP_006714247.1:p.Leu265=
XM_005262935.4:c.1190T= XP_005262992.1:p.Leu397=
XM_017008037.1:c.794T= XP_016863526.1:p.Leu265=
NM_207352.4:c.1190T= MANE Select NP_997235.3:p.Leu397=