Canonical Allele Identifier: CA2764875399
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186211361_186211363del , CM000666.2:g.186211361_186211363del GRCh38
NC_000004.11:g.187132515_187132517del , CM000666.1:g.187132515_187132517del GRCh37
NC_000004.10:g.187369509_187369511del NCBI36
NG_007965.1:g.24842_24844del
NG_012095.2:g.7383_7385del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.*720_*722del (CYP4V2) MANE Select ENSP00000368079.4:n.*720_*722del
ENST00000502665.1:n.1533_1535del (CYP4V2)
ENST00000507209.5:n.6996_6998del (CYP4V2)
ENST00000511608.5:c.201+2089_201+2091del (KLKB1)
NM_207352.3:c.*720_*722del (CYP4V2) NP_997235.3:n.*720_*722del
XM_005262935.2:c.*720_*722del (CYP4V2) XP_005262992.1:n.*720_*722del
XM_006714184.2:c.*720_*722del (CYP4V2) XP_006714247.1:n.*720_*722del
XM_011531931.1:c.-3348_-3346del (KLKB1) XP_011530233.1:n.-3348_-3346del
XM_011531932.1:c.-3598_-3596del (KLKB1) XP_011530234.1:n.-3598_-3596del
XM_011531933.1:c.-3412_-3410del (KLKB1) XP_011530235.1:n.-3412_-3410del
XM_005262935.4:c.*720_*722del (CYP4V2) XP_005262992.1:n.*720_*722del
XM_017008037.1:c.*720_*722del (CYP4V2) XP_016863526.1:n.*720_*722del
NM_207352.4:c.*720_*722del (CYP4V2) MANE Select NP_997235.3:n.*720_*722del