Canonical Allele Identifier: CA2581400249
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186210645T>A , CM000666.2:g.186210645T>A GRCh38
NC_000004.11:g.187131799T>A , CM000666.1:g.187131799T>A GRCh37
NC_000004.10:g.187368793T>A NCBI36
NG_007965.1:g.24126T>A
NG_012095.2:g.6667T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.*4T>A (CYP4V2) MANE Select ENSP00000368079.4:n.*4T>A
ENST00000378802.4:c.*4T>A (CYP4V2) ENSP00000368079.4:n.*4T>A
ENST00000502665.1:n.817T>A (CYP4V2)
ENST00000507209.5:n.6280T>A (CYP4V2)
ENST00000511608.5:c.201+1373T>A (KLKB1)
ENST00000513354.5:n.672T>A (CYP4V2)
NM_207352.3:c.*4T>A (CYP4V2) NP_997235.3:n.*4T>A
XM_005262935.2:c.*4T>A (CYP4V2) XP_005262992.1:n.*4T>A
XM_006714184.2:c.*4T>A (CYP4V2) XP_006714247.1:n.*4T>A
XM_005262935.4:c.*4T>A (CYP4V2) XP_005262992.1:n.*4T>A
XM_017008037.1:c.*4T>A (CYP4V2) XP_016863526.1:n.*4T>A
NM_207352.4:c.*4T>A (CYP4V2) MANE Select NP_997235.3:n.*4T>A
Search 100 bp 5'
Search 100 bp 3'