Canonical Allele Identifier: CA2672897286

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186197261-A-AGGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197261_186197262insGGTT , CM000666.2:g.186197261_186197262insGGTT	GRCh38
NC_000004.11:g.187118415_187118416insGGTT , CM000666.1:g.187118415_187118416insGGTT	GRCh37
NC_000004.10:g.187355409_187355410insGGTT	NCBI36
NG_007965.1:g.10742_10743insGGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.604+131_604+132insGGTT MANE Select	ENSP00000368079.4:n.604+131_604+132insGGTT
ENST00000378802.4:c.604+131_604+132insGGTT	ENSP00000368079.4:n.604+131_604+132insGGTT
ENST00000507209.5:n.1174_1175insGGTT
NM_207352.3:c.604+131_604+132insGGTT	NP_997235.3:n.604+131_604+132insGGTT
XM_005262935.2:c.604+131_604+132insGGTT	XP_005262992.1:n.604+131_604+132insGGTT
XM_006714184.2:c.208+131_208+132insGGTT	XP_006714247.1:n.208+131_208+132insGGTT
XM_005262935.4:c.604+131_604+132insGGTT	XP_005262992.1:n.604+131_604+132insGGTT
XM_017008037.1:c.208+131_208+132insGGTT	XP_016863526.1:n.208+131_208+132insGGTT
NM_207352.4:c.604+131_604+132insGGTT MANE Select	NP_997235.3:n.604+131_604+132insGGTT