Canonical Allele Identifier: CA358950509
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209173C>A , CM000666.2:g.186209173C>A GRCh38
NC_000004.11:g.187130327C>A , CM000666.1:g.187130327C>A GRCh37
NC_000004.10:g.187367321C>A NCBI36
NG_007965.1:g.22654C>A
NG_012095.2:g.5195C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1306C>A (CYP4V2) MANE Select ENSP00000368079.4:p.Pro436Thr
ENST00000378802.4:c.1306C>A (CYP4V2) ENSP00000368079.4:p.Pro436Thr
ENST00000502665.1:n.541C>A (CYP4V2)
ENST00000507209.5:n.6004C>A (CYP4V2)
ENST00000511608.5:c.102C>A (KLKB1)
ENST00000513354.5:n.396C>A (CYP4V2)
NM_207352.3:c.1306C>A (CYP4V2) NP_997235.3:p.Pro436Thr
XM_005262935.2:c.1303C>A (CYP4V2) XP_005262992.1:p.Pro435Thr
XM_006714184.2:c.910C>A (CYP4V2) XP_006714247.1:p.Pro304Thr
XM_005262935.4:c.1303C>A (CYP4V2) XP_005262992.1:p.Pro435Thr
XM_017008037.1:c.910C>A (CYP4V2) XP_016863526.1:p.Pro304Thr
NM_207352.4:c.1306C>A (CYP4V2) MANE Select NP_997235.3:p.Pro436Thr