Canonical Allele Identifier: CA2708145053

Gene: CYP4V2

Linked Data

• dbSNP Id: rs2126588914

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200693_186200705del , CM000666.2:g.186200693_186200705del	GRCh38
NC_000004.11:g.187121847_187121859del , CM000666.1:g.187121847_187121859del	GRCh37
NC_000004.10:g.187358841_187358853del	NCBI36
NG_007965.1:g.14174_14186del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-464_802-452del MANE Select	ENSP00000368079.4:n.802-464_802-452del
ENST00000378802.4:c.802-464_802-452del	ENSP00000368079.4:n.802-464_802-452del
ENST00000507209.5:n.1643-464_1643-452del
NM_207352.3:c.802-464_802-452del	NP_997235.3:n.802-464_802-452del
XM_005262935.2:c.802-464_802-452del	XP_005262992.1:n.802-464_802-452del
XM_006714184.2:c.406-464_406-452del	XP_006714247.1:n.406-464_406-452del
XM_005262935.4:c.802-464_802-452del	XP_005262992.1:n.802-464_802-452del
XM_017008037.1:c.406-464_406-452del	XP_016863526.1:n.406-464_406-452del
NM_207352.4:c.802-464_802-452del MANE Select	NP_997235.3:n.802-464_802-452del