Canonical Allele Identifier: CA1519888557
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186204831_186204835delinsCAGAT , CM000666.2:g.186204831_186204835delinsCAGAT GRCh38
NC_000004.11:g.187125985_187125989delinsCAGAT , CM000666.1:g.187125985_187125989delinsCAGAT GRCh37
NC_000004.10:g.187362979_187362983delinsCAGAT NCBI36
NG_007965.1:g.18312_18316delinsCAGAT
NG_012095.2:g.853_857delinsCAGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.988-369_988-365delinsCAGAT MANE Select ENSP00000368079.4:n.988-369_988-365delinsCAGAT
ENST00000378802.4:c.988-369_988-365delinsCAGAT ENSP00000368079.4:n.988-369_988-365delinsCAGAT
ENST00000507209.5:n.5317_5321delinsCAGAT
ENST00000513354.5:n.78-369_78-365delinsCAGAT
NM_207352.3:c.988-369_988-365delinsCAGAT NP_997235.3:n.988-369_988-365delinsCAGAT
XM_005262935.2:c.988-369_988-365delinsCAGAT XP_005262992.1:n.988-369_988-365delinsCAGAT
XM_006714184.2:c.592-369_592-365delinsCAGAT XP_006714247.1:n.592-369_592-365delinsCAGAT
XM_005262935.4:c.988-369_988-365delinsCAGAT XP_005262992.1:n.988-369_988-365delinsCAGAT
XM_017008037.1:c.592-369_592-365delinsCAGAT XP_016863526.1:n.592-369_592-365delinsCAGAT
NM_207352.4:c.988-369_988-365delinsCAGAT MANE Select NP_997235.3:n.988-369_988-365delinsCAGAT