Canonical Allele Identifier: CA2764875411
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186211373_186211374insA , CM000666.2:g.186211373_186211374insA GRCh38
NC_000004.11:g.187132527_187132528insA , CM000666.1:g.187132527_187132528insA GRCh37
NC_000004.10:g.187369521_187369522insA NCBI36
NG_007965.1:g.24854_24855insA
NG_012095.2:g.7395_7396insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.*732_*733insA (CYP4V2) MANE Select ENSP00000368079.4:n.*732_*733insA
ENST00000502665.1:n.1545_1546insA (CYP4V2)
ENST00000507209.5:n.7008_7009insA (CYP4V2)
ENST00000511608.5:c.201+2101_201+2102insA (KLKB1)
NM_207352.3:c.*732_*733insA (CYP4V2) NP_997235.3:n.*732_*733insA
XM_005262935.2:c.*732_*733insA (CYP4V2) XP_005262992.1:n.*732_*733insA
XM_006714184.2:c.*732_*733insA (CYP4V2) XP_006714247.1:n.*732_*733insA
XM_011531931.1:c.-3336_-3335insA (KLKB1) XP_011530233.1:n.-3336_-3335insA
XM_011531932.1:c.-3586_-3585insA (KLKB1) XP_011530234.1:n.-3586_-3585insA
XM_011531933.1:c.-3400_-3399insA (KLKB1) XP_011530235.1:n.-3400_-3399insA
XM_005262935.4:c.*732_*733insA (CYP4V2) XP_005262992.1:n.*732_*733insA
XM_017008037.1:c.*732_*733insA (CYP4V2) XP_016863526.1:n.*732_*733insA
NM_207352.4:c.*732_*733insA (CYP4V2) MANE Select NP_997235.3:n.*732_*733insA