Canonical Allele Identifier: CA2764868526

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200868_186201108del , CM000666.2:g.186200868_186201108del	GRCh38
NC_000004.11:g.187122022_187122262del , CM000666.1:g.187122022_187122262del	GRCh37
NC_000004.10:g.187359016_187359256del	NCBI36
NG_007965.1:g.14349_14589del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-289_802-49del MANE Select	ENSP00000368079.4:n.802-289_802-49del
ENST00000378802.4:c.802-289_802-49del	ENSP00000368079.4:n.802-289_802-49del
ENST00000507209.5:n.1643-289_1643-49del
NM_207352.3:c.802-289_802-49del	NP_997235.3:n.802-289_802-49del
XM_005262935.2:c.802-289_802-49del	XP_005262992.1:n.802-289_802-49del
XM_006714184.2:c.406-289_406-49del	XP_006714247.1:n.406-289_406-49del
XM_005262935.4:c.802-289_802-49del	XP_005262992.1:n.802-289_802-49del
XM_017008037.1:c.406-289_406-49del	XP_016863526.1:n.406-289_406-49del
NM_207352.4:c.802-289_802-49del MANE Select	NP_997235.3:n.802-289_802-49del