Canonical Allele Identifier: CA1519892061
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186210499C= , CM000666.2:g.186210499C= GRCh38
NC_000004.11:g.187131653C= , CM000666.1:g.187131653C= GRCh37
NC_000004.10:g.187368647C= NCBI36
NG_007965.1:g.23980C=
NG_012095.2:g.6521C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.1436C= (CYP4V2) MANE Select ENSP00000368079.4:p.Thr479=
ENST00000378802.4:c.1436C= (CYP4V2) ENSP00000368079.4:p.Thr479=
ENST00000502665.1:n.671C= (CYP4V2)
ENST00000507209.5:n.6134C= (CYP4V2)
ENST00000511608.5:c.201+1227C= (KLKB1)
ENST00000513354.5:n.526C= (CYP4V2)
NM_207352.3:c.1436C= (CYP4V2) NP_997235.3:p.Thr479=
XM_005262935.2:c.1433C= (CYP4V2) XP_005262992.1:p.Thr478=
XM_006714184.2:c.1040C= (CYP4V2) XP_006714247.1:p.Thr347=
XM_005262935.4:c.1433C= (CYP4V2) XP_005262992.1:p.Thr478=
XM_017008037.1:c.1040C= (CYP4V2) XP_016863526.1:p.Thr347=
NM_207352.4:c.1436C= (CYP4V2) MANE Select NP_997235.3:p.Thr479=