Canonical Allele Identifier: CA358950491
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209165T>A , CM000666.2:g.186209165T>A GRCh38
NC_000004.11:g.187130319T>A , CM000666.1:g.187130319T>A GRCh37
NC_000004.10:g.187367313T>A NCBI36
NG_007965.1:g.22646T>A
NG_012095.2:g.5187T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1298T>A (CYP4V2) MANE Select ENSP00000368079.4:p.Phe433Tyr
ENST00000378802.4:c.1298T>A (CYP4V2) ENSP00000368079.4:p.Phe433Tyr
ENST00000502665.1:n.533T>A (CYP4V2)
ENST00000507209.5:n.5996T>A (CYP4V2)
ENST00000511608.5:c.94T>A (KLKB1)
ENST00000513354.5:n.388T>A (CYP4V2)
NM_207352.3:c.1298T>A (CYP4V2) NP_997235.3:p.Phe433Tyr
XM_005262935.2:c.1295T>A (CYP4V2) XP_005262992.1:p.Phe432Tyr
XM_006714184.2:c.902T>A (CYP4V2) XP_006714247.1:p.Phe301Tyr
XM_005262935.4:c.1295T>A (CYP4V2) XP_005262992.1:p.Phe432Tyr
XM_017008037.1:c.902T>A (CYP4V2) XP_016863526.1:p.Phe301Tyr
NM_207352.4:c.1298T>A (CYP4V2) MANE Select NP_997235.3:p.Phe433Tyr