Canonical Allele Identifier: CA2764868805
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209060_186209061insACA , CM000666.2:g.186209060_186209061insACA GRCh38
NC_000004.11:g.187130214_187130215insACA , CM000666.1:g.187130214_187130215insACA GRCh37
NC_000004.10:g.187367208_187367209insACA NCBI36
NG_007965.1:g.22541_22542insACA
NG_012095.2:g.5082_5083insACA

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1226-33_1226-32insACA (CYP4V2) MANE Select ENSP00000368079.4:n.1226-33_1226-32insACA
ENST00000378802.4:c.1226-33_1226-32insACA (CYP4V2) ENSP00000368079.4:n.1226-33_1226-32insACA
ENST00000502665.1:n.461-33_461-32insACA (CYP4V2)
ENST00000507209.5:n.5924-33_5924-32insACA (CYP4V2)
ENST00000511608.5:c.22-33_22-32insACA (KLKB1)
ENST00000513354.5:n.316-33_316-32insACA (CYP4V2)
NM_207352.3:c.1226-33_1226-32insACA (CYP4V2) NP_997235.3:n.1226-33_1226-32insACA
XM_005262935.2:c.1226-36_1226-35insACA (CYP4V2) XP_005262992.1:n.1226-36_1226-35insACA
XM_006714184.2:c.830-33_830-32insACA (CYP4V2) XP_006714247.1:n.830-33_830-32insACA
XM_005262935.4:c.1226-36_1226-35insACA (CYP4V2) XP_005262992.1:n.1226-36_1226-35insACA
XM_017008037.1:c.830-33_830-32insACA (CYP4V2) XP_016863526.1:n.830-33_830-32insACA
NM_207352.4:c.1226-33_1226-32insACA (CYP4V2) MANE Select NP_997235.3:n.1226-33_1226-32insACA