Canonical Allele Identifier: CA1519891479
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209224C= , CM000666.2:g.186209224C= GRCh38
NC_000004.11:g.187130378C= , CM000666.1:g.187130378C= GRCh37
NC_000004.10:g.187367372C= NCBI36
NG_007965.1:g.22705C=
NG_012095.2:g.5246C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1357C= (CYP4V2) MANE Select ENSP00000368079.4:p.His453=
ENST00000378802.4:c.1357C= (CYP4V2) ENSP00000368079.4:p.His453=
ENST00000502665.1:n.592C= (CYP4V2)
ENST00000507209.5:n.6055C= (CYP4V2)
ENST00000511608.5:c.153C= (KLKB1)
ENST00000513354.5:n.447C= (CYP4V2)
NM_207352.3:c.1357C= (CYP4V2) NP_997235.3:p.His453=
XM_005262935.2:c.1354C= (CYP4V2) XP_005262992.1:p.His452=
XM_006714184.2:c.961C= (CYP4V2) XP_006714247.1:p.His321=
XM_005262935.4:c.1354C= (CYP4V2) XP_005262992.1:p.His452=
XM_017008037.1:c.961C= (CYP4V2) XP_016863526.1:p.His321=
NM_207352.4:c.1357C= (CYP4V2) MANE Select NP_997235.3:p.His453=