Canonical Allele Identifier: CA1519920341
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186198752_186198764delinsAAGAGCCCATTAT , CM000666.2:g.186198752_186198764delinsAAGAGCCCATTAT GRCh38
NC_000004.11:g.187119906_187119918delinsAAGAGCCCATTAT , CM000666.1:g.187119906_187119918delinsAAGAGCCCATTAT GRCh37
NC_000004.10:g.187356900_187356912delinsAAGAGCCCATTAT NCBI36
NG_007965.1:g.12233_12245delinsAAGAGCCCATTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.675-205_675-193delinsAAGAGCCCATTAT MANE Select ENSP00000368079.4:n.675-205_675-193delinsAAGAGCCCATTAT
ENST00000378802.4:c.675-205_675-193delinsAAGAGCCCATTAT ENSP00000368079.4:n.675-205_675-193delinsAAGAGCCCATTAT
ENST00000507209.5:n.1516-205_1516-193delinsAAGAGCCCATTAT
NM_207352.3:c.675-205_675-193delinsAAGAGCCCATTAT NP_997235.3:n.675-205_675-193delinsAAGAGCCCATTAT
XM_005262935.2:c.675-205_675-193delinsAAGAGCCCATTAT XP_005262992.1:n.675-205_675-193delinsAAGAGCCCATTAT
XM_006714184.2:c.279-205_279-193delinsAAGAGCCCATTAT XP_006714247.1:n.279-205_279-193delinsAAGAGCCCATTAT
XM_005262935.4:c.675-205_675-193delinsAAGAGCCCATTAT XP_005262992.1:n.675-205_675-193delinsAAGAGCCCATTAT
XM_017008037.1:c.279-205_279-193delinsAAGAGCCCATTAT XP_016863526.1:n.279-205_279-193delinsAAGAGCCCATTAT
NM_207352.4:c.675-205_675-193delinsAAGAGCCCATTAT MANE Select NP_997235.3:n.675-205_675-193delinsAAGAGCCCATTAT