Canonical Allele Identifier: CA2672897558
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209057_186209062dup , CM000666.2:g.186209057_186209062dup GRCh38
NC_000004.11:g.187130211_187130216dup , CM000666.1:g.187130211_187130216dup GRCh37
NC_000004.10:g.187367205_187367210dup NCBI36
NG_007965.1:g.22538_22543dup
NG_012095.2:g.5079_5084dup

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1226-36_1226-31dup (CYP4V2) MANE Select ENSP00000368079.4:n.1226-36_1226-31dup
ENST00000378802.4:c.1226-36_1226-31dup (CYP4V2) ENSP00000368079.4:n.1226-36_1226-31dup
ENST00000502665.1:n.461-36_461-31dup (CYP4V2)
ENST00000507209.5:n.5924-36_5924-31dup (CYP4V2)
ENST00000511608.5:c.22-36_22-31dup (KLKB1)
ENST00000513354.5:n.316-36_316-31dup (CYP4V2)
NM_207352.3:c.1226-36_1226-31dup (CYP4V2) NP_997235.3:n.1226-36_1226-31dup
XM_005262935.2:c.1226-39_1226-34dup (CYP4V2) XP_005262992.1:n.1226-39_1226-34dup
XM_006714184.2:c.830-36_830-31dup (CYP4V2) XP_006714247.1:n.830-36_830-31dup
XM_005262935.4:c.1226-39_1226-34dup (CYP4V2) XP_005262992.1:n.1226-39_1226-34dup
XM_017008037.1:c.830-36_830-31dup (CYP4V2) XP_016863526.1:n.830-36_830-31dup
NM_207352.4:c.1226-36_1226-31dup (CYP4V2) MANE Select NP_997235.3:n.1226-36_1226-31dup