Canonical Allele Identifier: CA1519892143
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186210675_186210678delinsAGGT , CM000666.2:g.186210675_186210678delinsAGGT GRCh38
NC_000004.11:g.187131829_187131832delinsAGGT , CM000666.1:g.187131829_187131832delinsAGGT GRCh37
NC_000004.10:g.187368823_187368826delinsAGGT NCBI36
NG_007965.1:g.24156_24159delinsAGGT
NG_012095.2:g.6697_6700delinsAGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.*34_*37delinsAGGT (CYP4V2) MANE Select ENSP00000368079.4:n.*34_*37delinsAGGT
ENST00000378802.4:c.*34_*37delinsAGGT (CYP4V2) ENSP00000368079.4:n.*34_*37delinsAGGT
ENST00000502665.1:n.847_850delinsAGGT (CYP4V2)
ENST00000507209.5:n.6310_6313delinsAGGT (CYP4V2)
ENST00000511608.5:c.201+1403_201+1406delinsAGGT (KLKB1)
ENST00000513354.5:n.702_705delinsAGGT (CYP4V2)
NM_207352.3:c.*34_*37delinsAGGT (CYP4V2) NP_997235.3:n.*34_*37delinsAGGT
XM_005262935.2:c.*34_*37delinsAGGT (CYP4V2) XP_005262992.1:n.*34_*37delinsAGGT
XM_006714184.2:c.*34_*37delinsAGGT (CYP4V2) XP_006714247.1:n.*34_*37delinsAGGT
XM_005262935.4:c.*34_*37delinsAGGT (CYP4V2) XP_005262992.1:n.*34_*37delinsAGGT
XM_017008037.1:c.*34_*37delinsAGGT (CYP4V2) XP_016863526.1:n.*34_*37delinsAGGT
NM_207352.4:c.*34_*37delinsAGGT (CYP4V2) MANE Select NP_997235.3:n.*34_*37delinsAGGT