Canonical Allele Identifier: CA2764867068
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194332_186194402del , CM000666.2:g.186194332_186194402del GRCh38
NC_000004.11:g.187115486_187115556del , CM000666.1:g.187115486_187115556del GRCh37
NC_000004.10:g.187352480_187352550del NCBI36
NG_007965.1:g.7813_7883del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.215-168_215-98del MANE Select ENSP00000368079.4:n.215-168_215-98del
ENST00000378802.4:c.215-168_215-98del ENSP00000368079.4:n.215-168_215-98del
NM_207352.3:c.215-168_215-98del NP_997235.3:n.215-168_215-98del
XM_005262935.2:c.215-168_215-98del XP_005262992.1:n.215-168_215-98del
XM_005262935.4:c.215-168_215-98del XP_005262992.1:n.215-168_215-98del
XM_017008037.1:c.-96-168_-96-98del XP_016863526.1:n.-96-168_-96-98del
NM_207352.4:c.215-168_215-98del MANE Select NP_997235.3:n.215-168_215-98del