Canonical Allele Identifier: CA1519888898
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205163_186205165delinsACT , CM000666.2:g.186205163_186205165delinsACT GRCh38
NC_000004.11:g.187126317_187126319delinsACT , CM000666.1:g.187126317_187126319delinsACT GRCh37
NC_000004.10:g.187363311_187363313delinsACT NCBI36
NG_007965.1:g.18644_18646delinsACT
NG_012095.2:g.1185_1187delinsACT

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.988-37_988-35delinsACT MANE Select ENSP00000368079.4:n.988-37_988-35delinsAC...
ENST00000378802.4:c.988-37_988-35delinsACT ENSP00000368079.4:n.988-37_988-35delinsAC...
ENST00000502665.1:n.223-37_223-35delinsACT
ENST00000507209.5:n.5649_5651delinsACT
ENST00000513354.5:n.78-37_78-35delinsACT
NM_207352.3:c.988-37_988-35delinsACT NP_997235.3:n.988-37_988-35delinsACT
XM_005262935.2:c.988-37_988-35delinsACT XP_005262992.1:n.988-37_988-35delinsACT
XM_006714184.2:c.592-37_592-35delinsACT XP_006714247.1:n.592-37_592-35delinsACT
XM_005262935.4:c.988-37_988-35delinsACT XP_005262992.1:n.988-37_988-35delinsACT
XM_017008037.1:c.592-37_592-35delinsACT XP_016863526.1:n.592-37_592-35delinsACT
NM_207352.4:c.988-37_988-35delinsACT MANE Select NP_997235.3:n.988-37_988-35delinsACT