Canonical Allele Identifier: CA2533297415
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186200862_186200863insTAC , CM000666.2:g.186200862_186200863insTAC GRCh38
NC_000004.11:g.187122016_187122017insTAC , CM000666.1:g.187122016_187122017insTAC GRCh37
NC_000004.10:g.187359010_187359011insTAC NCBI36
NG_007965.1:g.14343_14344insTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.802-295_802-294insTAC MANE Select ENSP00000368079.4:n.802-295_802-294insTAC
ENST00000378802.4:c.802-295_802-294insTAC ENSP00000368079.4:n.802-295_802-294insTAC
ENST00000507209.5:n.1643-295_1643-294insTAC
NM_207352.3:c.802-295_802-294insTAC NP_997235.3:n.802-295_802-294insTAC
XM_005262935.2:c.802-295_802-294insTAC XP_005262992.1:n.802-295_802-294insTAC
XM_006714184.2:c.406-295_406-294insTAC XP_006714247.1:n.406-295_406-294insTAC
XM_005262935.4:c.802-295_802-294insTAC XP_005262992.1:n.802-295_802-294insTAC
XM_017008037.1:c.406-295_406-294insTAC XP_016863526.1:n.406-295_406-294insTAC
NM_207352.4:c.802-295_802-294insTAC MANE Select NP_997235.3:n.802-295_802-294insTAC