Canonical Allele Identifier: CA1519883973

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200791_186200792delinsAT , CM000666.2:g.186200791_186200792delinsAT	GRCh38
NC_000004.11:g.187121945_187121946delinsAT , CM000666.1:g.187121945_187121946delinsAT	GRCh37
NC_000004.10:g.187358939_187358940delinsAT	NCBI36
NG_007965.1:g.14272_14273delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-366_802-365delinsAT MANE Select	ENSP00000368079.4:n.802-366_802-365delinsAT
ENST00000378802.4:c.802-366_802-365delinsAT	ENSP00000368079.4:n.802-366_802-365delinsAT
ENST00000507209.5:n.1643-366_1643-365delinsAT
NM_207352.3:c.802-366_802-365delinsAT	NP_997235.3:n.802-366_802-365delinsAT
XM_005262935.2:c.802-366_802-365delinsAT	XP_005262992.1:n.802-366_802-365delinsAT
XM_006714184.2:c.406-366_406-365delinsAT	XP_006714247.1:n.406-366_406-365delinsAT
XM_005262935.4:c.802-366_802-365delinsAT	XP_005262992.1:n.802-366_802-365delinsAT
XM_017008037.1:c.406-366_406-365delinsAT	XP_016863526.1:n.406-366_406-365delinsAT
NM_207352.4:c.802-366_802-365delinsAT MANE Select	NP_997235.3:n.802-366_802-365delinsAT