Canonical Allele Identifier: CA358950436
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209140G>C , CM000666.2:g.186209140G>C GRCh38
NC_000004.11:g.187130294G>C , CM000666.1:g.187130294G>C GRCh37
NC_000004.10:g.187367288G>C NCBI36
NG_007965.1:g.22621G>C
NG_012095.2:g.5162G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1273G>C (CYP4V2) MANE Select ENSP00000368079.4:p.Ala425Pro
ENST00000378802.4:c.1273G>C (CYP4V2) ENSP00000368079.4:p.Ala425Pro
ENST00000502665.1:n.508G>C (CYP4V2)
ENST00000507209.5:n.5971G>C (CYP4V2)
ENST00000511608.5:c.69G>C (KLKB1)
ENST00000513354.5:n.363G>C (CYP4V2)
NM_207352.3:c.1273G>C (CYP4V2) NP_997235.3:p.Ala425Pro
XM_005262935.2:c.1270G>C (CYP4V2) XP_005262992.1:p.Ala424Pro
XM_006714184.2:c.877G>C (CYP4V2) XP_006714247.1:p.Ala293Pro
XM_005262935.4:c.1270G>C (CYP4V2) XP_005262992.1:p.Ala424Pro
XM_017008037.1:c.877G>C (CYP4V2) XP_016863526.1:p.Ala293Pro
NM_207352.4:c.1273G>C (CYP4V2) MANE Select NP_997235.3:p.Ala425Pro