Canonical Allele Identifier: CA1519910325
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186191709_186191710delinsGA , CM000666.2:g.186191709_186191710delinsGA GRCh38
NC_000004.11:g.187112863_187112864delinsGA , CM000666.1:g.187112863_187112864delinsGA GRCh37
NC_000004.10:g.187349857_187349858delinsGA NCBI36
NG_007965.1:g.5190_5191delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.-115_-114delinsGA MANE Select ENSP00000368079.4:n.-115_-114delinsGA
ENST00000378802.4:c.-115_-114delinsGA ENSP00000368079.4:n.-115_-114delinsGA
NM_207352.3:c.-115_-114delinsGA NP_997235.3:n.-115_-114delinsGA
XM_005262935.2:c.-115_-114delinsGA XP_005262992.1:n.-115_-114delinsGA
XM_017008037.1:c.-425_-424delinsGA XP_016863526.1:n.-425_-424delinsGA
NM_207352.4:c.-115_-114delinsGA MANE Select NP_997235.3:n.-115_-114delinsGA