Canonical Allele Identifier: CA1519914802
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194391_186194393delinsCAT , CM000666.2:g.186194391_186194393delinsCAT GRCh38
NC_000004.11:g.187115545_187115547delinsCAT , CM000666.1:g.187115545_187115547delinsCAT GRCh37
NC_000004.10:g.187352539_187352541delinsCAT NCBI36
NG_007965.1:g.7872_7874delinsCAT

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.215-109_215-107delinsCAT MANE Select ENSP00000368079.4:n.215-109_215-107delins...
ENST00000378802.4:c.215-109_215-107delinsCAT ENSP00000368079.4:n.215-109_215-107delins...
NM_207352.3:c.215-109_215-107delinsCAT NP_997235.3:n.215-109_215-107delinsCAT
XM_005262935.2:c.215-109_215-107delinsCAT XP_005262992.1:n.215-109_215-107delinsCAT...
XM_005262935.4:c.215-109_215-107delinsCAT XP_005262992.1:n.215-109_215-107delinsCAT...
XM_017008037.1:c.-96-109_-96-107delinsCAT XP_016863526.1:n.-96-109_-96-107delinsCAT...
NM_207352.4:c.215-109_215-107delinsCAT MANE Select NP_997235.3:n.215-109_215-107delinsCAT