Canonical Allele Identifier: CA2764868329
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199093_186199094insA , CM000666.2:g.186199093_186199094insA GRCh38
NC_000004.11:g.187120247_187120248insA , CM000666.1:g.187120247_187120248insA GRCh37
NC_000004.10:g.187357241_187357242insA NCBI36
NG_007965.1:g.12574_12575insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.801+10_801+11insA MANE Select ENSP00000368079.4:n.801+10_801+11insA
ENST00000378802.4:c.801+10_801+11insA ENSP00000368079.4:n.801+10_801+11insA
ENST00000507209.5:n.1642+10_1642+11insA
NM_207352.3:c.801+10_801+11insA NP_997235.3:n.801+10_801+11insA
XM_005262935.2:c.801+10_801+11insA XP_005262992.1:n.801+10_801+11insA
XM_006714184.2:c.405+10_405+11insA XP_006714247.1:n.405+10_405+11insA
XM_005262935.4:c.801+10_801+11insA XP_005262992.1:n.801+10_801+11insA
XM_017008037.1:c.405+10_405+11insA XP_016863526.1:n.405+10_405+11insA
NM_207352.4:c.801+10_801+11insA MANE Select NP_997235.3:n.801+10_801+11insA
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