Canonical Allele Identifier: CA2764867895
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197263_186197264insTTCTGAGGA , CM000666.2:g.186197263_186197264insTTCTGAGGA GRCh38
NC_000004.11:g.187118417_187118418insTTCTGAGGA , CM000666.1:g.187118417_187118418insTTCTGAGGA GRCh37
NC_000004.10:g.187355411_187355412insTTCTGAGGA NCBI36
NG_007965.1:g.10744_10745insTTCTGAGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.604+133_604+134insTTCTGAGGA MANE Select ENSP00000368079.4:n.604+133_604+134insTTCTGAGGA
ENST00000378802.4:c.604+133_604+134insTTCTGAGGA ENSP00000368079.4:n.604+133_604+134insTTCTGAGGA
ENST00000507209.5:n.1176_1177insTTCTGAGGA
NM_207352.3:c.604+133_604+134insTTCTGAGGA NP_997235.3:n.604+133_604+134insTTCTGAGGA
XM_005262935.2:c.604+133_604+134insTTCTGAGGA XP_005262992.1:n.604+133_604+134insTTCTGAGGA
XM_006714184.2:c.208+133_208+134insTTCTGAGGA XP_006714247.1:n.208+133_208+134insTTCTGAGGA
XM_005262935.4:c.604+133_604+134insTTCTGAGGA XP_005262992.1:n.604+133_604+134insTTCTGAGGA
XM_017008037.1:c.208+133_208+134insTTCTGAGGA XP_016863526.1:n.208+133_208+134insTTCTGAGGA
NM_207352.4:c.604+133_604+134insTTCTGAGGA MANE Select NP_997235.3:n.604+133_604+134insTTCTGAGGA