Canonical Allele Identifier: CA2672897508
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208979_186208987del , CM000666.2:g.186208979_186208987del GRCh38
NC_000004.11:g.187130133_187130141del , CM000666.1:g.187130133_187130141del GRCh37
NC_000004.10:g.187367127_187367135del NCBI36
NG_007965.1:g.22460_22468del
NG_012095.2:g.5001_5009del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1205_1213del MANE Select ENSP00000368079.4:p.Val402_Glu404del
ENST00000378802.4:c.1205_1213del ENSP00000368079.4:p.Val402_Glu404del
ENST00000502665.1:n.440_448del
ENST00000507209.5:n.5903_5911del
ENST00000513354.5:n.295_303del
NM_207352.3:c.1205_1213del NP_997235.3:p.Val402_Glu404del
XM_005262935.2:c.1205_1213del XP_005262992.1:p.Val402_Glu404del
XM_006714184.2:c.809_817del XP_006714247.1:p.Val270_Glu272del
XM_005262935.4:c.1205_1213del XP_005262992.1:p.Val402_Glu404del
XM_017008037.1:c.809_817del XP_016863526.1:p.Val270_Glu272del
NM_207352.4:c.1205_1213del MANE Select NP_997235.3:p.Val402_Glu404del