Canonical Allele Identifier: CA2672898111
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186210350_186210351insCCATTCTGA , CM000666.2:g.186210350_186210351insCCATTCTGA GRCh38
NC_000004.11:g.187131504_187131505insCCATTCTGA , CM000666.1:g.187131504_187131505insCCATTCTGA GRCh37
NC_000004.10:g.187368498_187368499insCCATTCTGA NCBI36
NG_007965.1:g.23831_23832insCCATTCTGA
NG_012095.2:g.6372_6373insCCATTCTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.1406-119_1406-118insCCATTCTGA (CYP4V2) MANE Select ENSP00000368079.4:n.1406-119_1406-118insCCATTCTGA
ENST00000378802.4:c.1406-119_1406-118insCCATTCTGA (CYP4V2) ENSP00000368079.4:n.1406-119_1406-118insCCATTCTGA
ENST00000502665.1:n.641-119_641-118insCCATTCTGA (CYP4V2)
ENST00000507209.5:n.6104-119_6104-118insCCATTCTGA (CYP4V2)
ENST00000511608.5:c.201+1078_201+1079insCCATTCTGA (KLKB1)
ENST00000513354.5:n.496-119_496-118insCCATTCTGA (CYP4V2)
NM_207352.3:c.1406-119_1406-118insCCATTCTGA (CYP4V2) NP_997235.3:n.1406-119_1406-118insCCATTCTGA
XM_005262935.2:c.1403-119_1403-118insCCATTCTGA (CYP4V2) XP_005262992.1:n.1403-119_1403-118insCCATTCTGA
XM_006714184.2:c.1010-119_1010-118insCCATTCTGA (CYP4V2) XP_006714247.1:n.1010-119_1010-118insCCATTCTGA
XM_005262935.4:c.1403-119_1403-118insCCATTCTGA (CYP4V2) XP_005262992.1:n.1403-119_1403-118insCCATTCTGA
XM_017008037.1:c.1010-119_1010-118insCCATTCTGA (CYP4V2) XP_016863526.1:n.1010-119_1010-118insCCATTCTGA
NM_207352.4:c.1406-119_1406-118insCCATTCTGA (CYP4V2) MANE Select NP_997235.3:n.1406-119_1406-118insCCATTCTGA