Canonical Allele Identifier: CA1519893859
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186212800G= , CM000666.2:g.186212800G= GRCh38
NC_000004.11:g.187133954G= , CM000666.1:g.187133954G= GRCh37
NC_000004.10:g.187370948G= NCBI36
NG_007965.1:g.26281G=
NG_012095.2:g.8822G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.*2159G= (CYP4V2) MANE Select ENSP00000368079.4:n.*2159G=
ENST00000502665.1:n.2972G= (CYP4V2)
ENST00000507209.5:n.8435G= (CYP4V2)
ENST00000511608.5:c.201+3528G= (KLKB1)
NM_207352.3:c.*2159G= (CYP4V2) NP_997235.3:n.*2159G=
XM_005262935.2:c.*2159G= (CYP4V2) XP_005262992.1:n.*2159G=
XM_006714184.2:c.*2159G= (CYP4V2) XP_006714247.1:n.*2159G=
XM_011531931.1:c.-1909G= (KLKB1) XP_011530233.1:n.-1909G=
XM_011531932.1:c.-2159G= (KLKB1) XP_011530234.1:n.-2159G=
XM_011531933.1:c.-1973G= (KLKB1) XP_011530235.1:n.-1973G=
XM_005262935.4:c.*2159G= (CYP4V2) XP_005262992.1:n.*2159G=
XM_017008037.1:c.*2159G= (CYP4V2) XP_016863526.1:n.*2159G=
NM_207352.4:c.*2159G= (CYP4V2) MANE Select NP_997235.3:n.*2159G=