Canonical Allele Identifier: CA2764867686
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186204664del , CM000666.2:g.186204664del GRCh38
NC_000004.11:g.187125818del , CM000666.1:g.187125818del GRCh37
NC_000004.10:g.187362812del NCBI36
NG_007965.1:g.18145del
NG_012095.2:g.686del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.988-536del MANE Select ENSP00000368079.4:n.988-536del
ENST00000378802.4:c.988-536del ENSP00000368079.4:n.988-536del
ENST00000507209.5:n.5150del
ENST00000513354.5:n.77+207del
NM_207352.3:c.988-536del NP_997235.3:n.988-536del
XM_005262935.2:c.988-536del XP_005262992.1:n.988-536del
XM_006714184.2:c.592-536del XP_006714247.1:n.592-536del
XM_005262935.4:c.988-536del XP_005262992.1:n.988-536del
XM_017008037.1:c.592-536del XP_016863526.1:n.592-536del
NM_207352.4:c.988-536del MANE Select NP_997235.3:n.988-536del