Canonical Allele Identifier: CA2672896420
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186204895_186204899del , CM000666.2:g.186204895_186204899del GRCh38
NC_000004.11:g.187126049_187126053del , CM000666.1:g.187126049_187126053del GRCh37
NC_000004.10:g.187363043_187363047del NCBI36
NG_007965.1:g.18376_18380del
NG_012095.2:g.917_921del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.988-305_988-301del MANE Select ENSP00000368079.4:n.988-305_988-301del
ENST00000378802.4:c.988-305_988-301del ENSP00000368079.4:n.988-305_988-301del
ENST00000502665.1:n.59_63del
ENST00000507209.5:n.5381_5385del
ENST00000513354.5:n.78-305_78-301del
NM_207352.3:c.988-305_988-301del NP_997235.3:n.988-305_988-301del
XM_005262935.2:c.988-305_988-301del XP_005262992.1:n.988-305_988-301del
XM_006714184.2:c.592-305_592-301del XP_006714247.1:n.592-305_592-301del
XM_005262935.4:c.988-305_988-301del XP_005262992.1:n.988-305_988-301del
XM_017008037.1:c.592-305_592-301del XP_016863526.1:n.592-305_592-301del
NM_207352.4:c.988-305_988-301del MANE Select NP_997235.3:n.988-305_988-301del