Canonical Allele Identifier: CA2764867965
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197695_186197697del , CM000666.2:g.186197695_186197697del GRCh38
NC_000004.11:g.187118849_187118851del , CM000666.1:g.187118849_187118851del GRCh37
NC_000004.10:g.187355843_187355845del NCBI36
NG_007965.1:g.11176_11178del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.674+93_674+95del MANE Select ENSP00000368079.4:n.674+93_674+95del
ENST00000378802.4:c.674+93_674+95del ENSP00000368079.4:n.674+93_674+95del
ENST00000507209.5:n.1515+93_1515+95del
NM_207352.3:c.674+93_674+95del NP_997235.3:n.674+93_674+95del
XM_005262935.2:c.674+93_674+95del XP_005262992.1:n.674+93_674+95del
XM_006714184.2:c.278+93_278+95del XP_006714247.1:n.278+93_278+95del
XM_005262935.4:c.674+93_674+95del XP_005262992.1:n.674+93_674+95del
XM_017008037.1:c.278+93_278+95del XP_016863526.1:n.278+93_278+95del
NM_207352.4:c.674+93_674+95del MANE Select NP_997235.3:n.674+93_674+95del