Canonical Allele Identifier: CA2672895977
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186204648_186204657del , CM000666.2:g.186204648_186204657del GRCh38
NC_000004.11:g.187125802_187125811del , CM000666.1:g.187125802_187125811del GRCh37
NC_000004.10:g.187362796_187362805del NCBI36
NG_007965.1:g.18129_18138del
NG_012095.2:g.670_679del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.988-552_988-543del MANE Select ENSP00000368079.4:n.988-552_988-543del
ENST00000378802.4:c.988-552_988-543del ENSP00000368079.4:n.988-552_988-543del
ENST00000507209.5:n.5134_5143del
ENST00000513354.5:n.77+191_77+200del
NM_207352.3:c.988-552_988-543del NP_997235.3:n.988-552_988-543del
XM_005262935.2:c.988-552_988-543del XP_005262992.1:n.988-552_988-543del
XM_006714184.2:c.592-552_592-543del XP_006714247.1:n.592-552_592-543del
XM_005262935.4:c.988-552_988-543del XP_005262992.1:n.988-552_988-543del
XM_017008037.1:c.592-552_592-543del XP_016863526.1:n.592-552_592-543del
NM_207352.4:c.988-552_988-543del MANE Select NP_997235.3:n.988-552_988-543del