Canonical Allele Identifier: CA1519883872
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186200664_186200690delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA , CM000666.2:g.186200664_186200690delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA GRCh38
NC_000004.11:g.187121818_187121844delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA , CM000666.1:g.187121818_187121844delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA GRCh37
NC_000004.10:g.187358812_187358838delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA NCBI36
NG_007965.1:g.14145_14171delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.802-493_802-467delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA MANE Select ENSP00000368079.4:n.802-493_802-467delinsGGAGGGGGCAGCCGTGCAGG...
ENST00000378802.4:c.802-493_802-467delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA ENSP00000368079.4:n.802-493_802-467delinsGGAGGGGGCAGCCGTGCAGG...
ENST00000507209.5:n.1643-493_1643-467delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA
NM_207352.3:c.802-493_802-467delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA NP_997235.3:n.802-493_802-467delinsGGAGGGGGCAGCCGTGCAGGCCTCTG...
XM_005262935.2:c.802-493_802-467delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA XP_005262992.1:n.802-493_802-467delinsGGAGGGGGCAGCCGTGCAGGCCT...
XM_006714184.2:c.406-493_406-467delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA XP_006714247.1:n.406-493_406-467delinsGGAGGGGGCAGCCGTGCAGGCCT...
XM_005262935.4:c.802-493_802-467delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA XP_005262992.1:n.802-493_802-467delinsGGAGGGGGCAGCCGTGCAGGCCT...
XM_017008037.1:c.406-493_406-467delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA XP_016863526.1:n.406-493_406-467delinsGGAGGGGGCAGCCGTGCAGGCCT...
NM_207352.4:c.802-493_802-467delinsGGAGGGGGCAGCCGTGCAGGCCTCTGA MANE Select NP_997235.3:n.802-493_802-467delinsGGAGGGGGCAGCCGTGCAGGCCTCTG...