Canonical Allele Identifier: CA2764868928
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209379_186209380insAGTC , CM000666.2:g.186209379_186209380insAGTC GRCh38
NC_000004.11:g.187130533_187130534insAGTC , CM000666.1:g.187130533_187130534insAGTC GRCh37
NC_000004.10:g.187367527_187367528insAGTC NCBI36
NG_007965.1:g.22860_22861insAGTC
NG_012095.2:g.5401_5402insAGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.1405+107_1405+108insAGTC (CYP4V2) MANE Select ENSP00000368079.4:n.1405+107_1405+108insAGTC
ENST00000378802.4:c.1405+107_1405+108insAGTC (CYP4V2) ENSP00000368079.4:n.1405+107_1405+108insAGTC
ENST00000502665.1:n.640+107_640+108insAGTC (CYP4V2)
ENST00000507209.5:n.6103+107_6103+108insAGTC (CYP4V2)
ENST00000511608.5:c.201+107_201+108insAGTC (KLKB1)
ENST00000513354.5:n.495+107_495+108insAGTC (CYP4V2)
NM_207352.3:c.1405+107_1405+108insAGTC (CYP4V2) NP_997235.3:n.1405+107_1405+108insAGTC
XM_005262935.2:c.1402+107_1402+108insAGTC (CYP4V2) XP_005262992.1:n.1402+107_1402+108insAGTC
XM_006714184.2:c.1009+107_1009+108insAGTC (CYP4V2) XP_006714247.1:n.1009+107_1009+108insAGTC
XM_005262935.4:c.1402+107_1402+108insAGTC (CYP4V2) XP_005262992.1:n.1402+107_1402+108insAGTC
XM_017008037.1:c.1009+107_1009+108insAGTC (CYP4V2) XP_016863526.1:n.1009+107_1009+108insAGTC
NM_207352.4:c.1405+107_1405+108insAGTC (CYP4V2) MANE Select NP_997235.3:n.1405+107_1405+108insAGTC