Canonical Allele Identifier: CA2764868412
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186199172_186199173insAGA , CM000666.2:g.186199172_186199173insAGA GRCh38
NC_000004.11:g.187120326_187120327insAGA , CM000666.1:g.187120326_187120327insAGA GRCh37
NC_000004.10:g.187357320_187357321insAGA NCBI36
NG_007965.1:g.12653_12654insAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.801+89_801+90insAGA MANE Select ENSP00000368079.4:n.801+89_801+90insAGA
ENST00000378802.4:c.801+89_801+90insAGA ENSP00000368079.4:n.801+89_801+90insAGA
ENST00000507209.5:n.1642+89_1642+90insAGA
NM_207352.3:c.801+89_801+90insAGA NP_997235.3:n.801+89_801+90insAGA
XM_005262935.2:c.801+89_801+90insAGA XP_005262992.1:n.801+89_801+90insAGA
XM_006714184.2:c.405+89_405+90insAGA XP_006714247.1:n.405+89_405+90insAGA
XM_005262935.4:c.801+89_801+90insAGA XP_005262992.1:n.801+89_801+90insAGA
XM_017008037.1:c.405+89_405+90insAGA XP_016863526.1:n.405+89_405+90insAGA
NM_207352.4:c.801+89_801+90insAGA MANE Select NP_997235.3:n.801+89_801+90insAGA
Search 100 bp 5'
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