Canonical Allele Identifier: CA2764867660
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186204653del , CM000666.2:g.186204653del GRCh38
NC_000004.11:g.187125807del , CM000666.1:g.187125807del GRCh37
NC_000004.10:g.187362801del NCBI36
NG_007965.1:g.18134del
NG_012095.2:g.675del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.988-547del MANE Select ENSP00000368079.4:n.988-547del
ENST00000378802.4:c.988-547del ENSP00000368079.4:n.988-547del
ENST00000507209.5:n.5139del
ENST00000513354.5:n.77+196del
NM_207352.3:c.988-547del NP_997235.3:n.988-547del
XM_005262935.2:c.988-547del XP_005262992.1:n.988-547del
XM_006714184.2:c.592-547del XP_006714247.1:n.592-547del
XM_005262935.4:c.988-547del XP_005262992.1:n.988-547del
XM_017008037.1:c.592-547del XP_016863526.1:n.592-547del
NM_207352.4:c.988-547del MANE Select NP_997235.3:n.988-547del