Canonical Allele Identifier: CA2764868397
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199166_186199167insACA , CM000666.2:g.186199166_186199167insACA GRCh38
NC_000004.11:g.187120320_187120321insACA , CM000666.1:g.187120320_187120321insACA GRCh37
NC_000004.10:g.187357314_187357315insACA NCBI36
NG_007965.1:g.12647_12648insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.801+83_801+84insACA MANE Select ENSP00000368079.4:n.801+83_801+84insACA
ENST00000378802.4:c.801+83_801+84insACA ENSP00000368079.4:n.801+83_801+84insACA
ENST00000507209.5:n.1642+83_1642+84insACA
NM_207352.3:c.801+83_801+84insACA NP_997235.3:n.801+83_801+84insACA
XM_005262935.2:c.801+83_801+84insACA XP_005262992.1:n.801+83_801+84insACA
XM_006714184.2:c.405+83_405+84insACA XP_006714247.1:n.405+83_405+84insACA
XM_005262935.4:c.801+83_801+84insACA XP_005262992.1:n.801+83_801+84insACA
XM_017008037.1:c.405+83_405+84insACA XP_016863526.1:n.405+83_405+84insACA
NM_207352.4:c.801+83_801+84insACA MANE Select NP_997235.3:n.801+83_801+84insACA
Search 100 bp 5'
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