Canonical Allele Identifier: CA1519892119
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186210637G= , CM000666.2:g.186210637G= GRCh38
NC_000004.11:g.187131791G= , CM000666.1:g.187131791G= GRCh37
NC_000004.10:g.187368785G= NCBI36
NG_007965.1:g.24118G=
NG_012095.2:g.6659G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.1574G= (CYP4V2) MANE Select ENSP00000368079.4:p.Arg525=
ENST00000378802.4:c.1574G= (CYP4V2) ENSP00000368079.4:p.Arg525=
ENST00000502665.1:n.809G= (CYP4V2)
ENST00000507209.5:n.6272G= (CYP4V2)
ENST00000511608.5:c.201+1365G= (KLKB1)
ENST00000513354.5:n.664G= (CYP4V2)
NM_207352.3:c.1574G= (CYP4V2) NP_997235.3:p.Arg525=
XM_005262935.2:c.1571G= (CYP4V2) XP_005262992.1:p.Arg524=
XM_006714184.2:c.1178G= (CYP4V2) XP_006714247.1:p.Arg393=
XM_005262935.4:c.1571G= (CYP4V2) XP_005262992.1:p.Arg524=
XM_017008037.1:c.1178G= (CYP4V2) XP_016863526.1:p.Arg393=
NM_207352.4:c.1574G= (CYP4V2) MANE Select NP_997235.3:p.Arg525=