Canonical Allele Identifier: CA1519920474
Gene: CYP4V2 HGNC NCBI

Linked Data

dbSNP Id: rs1736234824

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199076_186199078del , CM000666.2:g.186199076_186199078del GRCh38
NC_000004.11:g.187120230_187120232del , CM000666.1:g.187120230_187120232del GRCh37
NC_000004.10:g.187357224_187357226del NCBI36
NG_007965.1:g.12557_12559del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.794_796del MANE Select ENSP00000368079.4:p.Thr265del
ENST00000378802.4:c.794_796del ENSP00000368079.4:p.Thr265del
ENST00000507209.5:n.1635_1637del
NM_207352.3:c.794_796del NP_997235.3:p.Thr265del
XM_005262935.2:c.794_796del XP_005262992.1:p.Thr265del
XM_006714184.2:c.398_400del XP_006714247.1:p.Thr133del
XM_005262935.4:c.794_796del XP_005262992.1:p.Thr265del
XM_017008037.1:c.398_400del XP_016863526.1:p.Thr133del
NM_207352.4:c.794_796del MANE Select NP_997235.3:p.Thr265del