Canonical Allele Identifier: CA2764868381
Gene: CYP4V2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199146_186199157del , CM000666.2:g.186199146_186199157del GRCh38
NC_000004.11:g.187120300_187120311del , CM000666.1:g.187120300_187120311del GRCh37
NC_000004.10:g.187357294_187357305del NCBI36
NG_007965.1:g.12627_12638del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.801+63_801+74del MANE Select ENSP00000368079.4:n.801+63_801+74del
ENST00000378802.4:c.801+63_801+74del ENSP00000368079.4:n.801+63_801+74del
ENST00000507209.5:n.1642+63_1642+74del
NM_207352.3:c.801+63_801+74del NP_997235.3:n.801+63_801+74del
XM_005262935.2:c.801+63_801+74del XP_005262992.1:n.801+63_801+74del
XM_006714184.2:c.405+63_405+74del XP_006714247.1:n.405+63_405+74del
XM_005262935.4:c.801+63_801+74del XP_005262992.1:n.801+63_801+74del
XM_017008037.1:c.405+63_405+74del XP_016863526.1:n.405+63_405+74del
NM_207352.4:c.801+63_801+74del MANE Select NP_997235.3:n.801+63_801+74del
Search 100 bp 5'
Search 100 bp 3'