Canonical Allele Identifier: CA1519892064
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186210507T= , CM000666.2:g.186210507T= GRCh38
NC_000004.11:g.187131661T= , CM000666.1:g.187131661T= GRCh37
NC_000004.10:g.187368655T= NCBI36
NG_007965.1:g.23988T=
NG_012095.2:g.6529T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.1444T= (CYP4V2) MANE Select ENSP00000368079.4:p.Ser482=
ENST00000378802.4:c.1444T= (CYP4V2) ENSP00000368079.4:p.Ser482=
ENST00000502665.1:n.679T= (CYP4V2)
ENST00000507209.5:n.6142T= (CYP4V2)
ENST00000511608.5:c.201+1235T= (KLKB1)
ENST00000513354.5:n.534T= (CYP4V2)
NM_207352.3:c.1444T= (CYP4V2) NP_997235.3:p.Ser482=
XM_005262935.2:c.1441T= (CYP4V2) XP_005262992.1:p.Ser481=
XM_006714184.2:c.1048T= (CYP4V2) XP_006714247.1:p.Ser350=
XM_005262935.4:c.1441T= (CYP4V2) XP_005262992.1:p.Ser481=
XM_017008037.1:c.1048T= (CYP4V2) XP_016863526.1:p.Ser350=
NM_207352.4:c.1444T= (CYP4V2) MANE Select NP_997235.3:p.Ser482=