Canonical Allele Identifier: CA2764868401
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199168_186199169insA , CM000666.2:g.186199168_186199169insA GRCh38
NC_000004.11:g.187120322_187120323insA , CM000666.1:g.187120322_187120323insA GRCh37
NC_000004.10:g.187357316_187357317insA NCBI36
NG_007965.1:g.12649_12650insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.801+85_801+86insA MANE Select ENSP00000368079.4:n.801+85_801+86insA
ENST00000378802.4:c.801+85_801+86insA ENSP00000368079.4:n.801+85_801+86insA
ENST00000507209.5:n.1642+85_1642+86insA
NM_207352.3:c.801+85_801+86insA NP_997235.3:n.801+85_801+86insA
XM_005262935.2:c.801+85_801+86insA XP_005262992.1:n.801+85_801+86insA
XM_006714184.2:c.405+85_405+86insA XP_006714247.1:n.405+85_405+86insA
XM_005262935.4:c.801+85_801+86insA XP_005262992.1:n.801+85_801+86insA
XM_017008037.1:c.405+85_405+86insA XP_016863526.1:n.405+85_405+86insA
NM_207352.4:c.801+85_801+86insA MANE Select NP_997235.3:n.801+85_801+86insA
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