Canonical Allele Identifier: CA2672898280
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186210656_186210658dup , CM000666.2:g.186210656_186210658dup GRCh38
NC_000004.11:g.187131810_187131812dup , CM000666.1:g.187131810_187131812dup GRCh37
NC_000004.10:g.187368804_187368806dup NCBI36
NG_007965.1:g.24137_24139dup
NG_012095.2:g.6678_6680dup

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.*15_*17dup (CYP4V2) MANE Select ENSP00000368079.4:n.*15_*17dup
ENST00000378802.4:c.*15_*17dup (CYP4V2) ENSP00000368079.4:n.*15_*17dup
ENST00000502665.1:n.828_830dup (CYP4V2)
ENST00000507209.5:n.6291_6293dup (CYP4V2)
ENST00000511608.5:c.201+1384_201+1386dup (KLKB1)
ENST00000513354.5:n.683_685dup (CYP4V2)
NM_207352.3:c.*15_*17dup (CYP4V2) NP_997235.3:n.*15_*17dup
XM_005262935.2:c.*15_*17dup (CYP4V2) XP_005262992.1:n.*15_*17dup
XM_006714184.2:c.*15_*17dup (CYP4V2) XP_006714247.1:n.*15_*17dup
XM_005262935.4:c.*15_*17dup (CYP4V2) XP_005262992.1:n.*15_*17dup
XM_017008037.1:c.*15_*17dup (CYP4V2) XP_016863526.1:n.*15_*17dup
NM_207352.4:c.*15_*17dup (CYP4V2) MANE Select NP_997235.3:n.*15_*17dup