Canonical Allele Identifier: CA917387433
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

dbSNP Id: rs1561440759

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186212599_186212600del , CM000666.2:g.186212599_186212600del GRCh38
NC_000004.11:g.187133753_187133754del , CM000666.1:g.187133753_187133754del GRCh37
NC_000004.10:g.187370747_187370748del NCBI36
NG_007965.1:g.26080_26081del
NG_012095.2:g.8621_8622del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.*1958_*1959del (CYP4V2) MANE Select ENSP00000368079.4:n.*1958_*1959del
ENST00000502665.1:n.2771_2772del (CYP4V2)
ENST00000507209.5:n.8234_8235del (CYP4V2)
ENST00000511608.5:c.201+3327_201+3328del (KLKB1)
NM_207352.3:c.*1958_*1959del (CYP4V2) NP_997235.3:n.*1958_*1959del
XM_005262935.2:c.*1958_*1959del (CYP4V2) XP_005262992.1:n.*1958_*1959del
XM_006714184.2:c.*1958_*1959del (CYP4V2) XP_006714247.1:n.*1958_*1959del
XM_011531931.1:c.-2110_-2109del (KLKB1) XP_011530233.1:n.-2110_-2109del
XM_011531932.1:c.-2360_-2359del (KLKB1) XP_011530234.1:n.-2360_-2359del
XM_011531933.1:c.-2174_-2173del (KLKB1) XP_011530235.1:n.-2174_-2173del
XM_005262935.4:c.*1958_*1959del (CYP4V2) XP_005262992.1:n.*1958_*1959del
XM_017008037.1:c.*1958_*1959del (CYP4V2) XP_016863526.1:n.*1958_*1959del
NM_207352.4:c.*1958_*1959del (CYP4V2) MANE Select NP_997235.3:n.*1958_*1959del