Canonical Allele Identifier: CA2764868337
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199110_186199111del , CM000666.2:g.186199110_186199111del GRCh38
NC_000004.11:g.187120264_187120265del , CM000666.1:g.187120264_187120265del GRCh37
NC_000004.10:g.187357258_187357259del NCBI36
NG_007965.1:g.12591_12592del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.801+27_801+28del MANE Select ENSP00000368079.4:n.801+27_801+28del
ENST00000378802.4:c.801+27_801+28del ENSP00000368079.4:n.801+27_801+28del
ENST00000507209.5:n.1642+27_1642+28del
NM_207352.3:c.801+27_801+28del NP_997235.3:n.801+27_801+28del
XM_005262935.2:c.801+27_801+28del XP_005262992.1:n.801+27_801+28del
XM_006714184.2:c.405+27_405+28del XP_006714247.1:n.405+27_405+28del
XM_005262935.4:c.801+27_801+28del XP_005262992.1:n.801+27_801+28del
XM_017008037.1:c.405+27_405+28del XP_016863526.1:n.405+27_405+28del
NM_207352.4:c.801+27_801+28del MANE Select NP_997235.3:n.801+27_801+28del
Search 100 bp 5'
Search 100 bp 3'