Canonical Allele Identifier: CA358950482
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209161T>A , CM000666.2:g.186209161T>A GRCh38
NC_000004.11:g.187130315T>A , CM000666.1:g.187130315T>A GRCh37
NC_000004.10:g.187367309T>A NCBI36
NG_007965.1:g.22642T>A
NG_012095.2:g.5183T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1294T>A (CYP4V2) MANE Select ENSP00000368079.4:p.Tyr432Asn
ENST00000378802.4:c.1294T>A (CYP4V2) ENSP00000368079.4:p.Tyr432Asn
ENST00000502665.1:n.529T>A (CYP4V2)
ENST00000507209.5:n.5992T>A (CYP4V2)
ENST00000511608.5:c.90T>A (KLKB1)
ENST00000513354.5:n.384T>A (CYP4V2)
NM_207352.3:c.1294T>A (CYP4V2) NP_997235.3:p.Tyr432Asn
XM_005262935.2:c.1291T>A (CYP4V2) XP_005262992.1:p.Tyr431Asn
XM_006714184.2:c.898T>A (CYP4V2) XP_006714247.1:p.Tyr300Asn
XM_005262935.4:c.1291T>A (CYP4V2) XP_005262992.1:p.Tyr431Asn
XM_017008037.1:c.898T>A (CYP4V2) XP_016863526.1:p.Tyr300Asn
NM_207352.4:c.1294T>A (CYP4V2) MANE Select NP_997235.3:p.Tyr432Asn