Canonical Allele Identifier: CA2764867824

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197163_186197164insT , CM000666.2:g.186197163_186197164insT	GRCh38
NC_000004.11:g.187118317_187118318insT , CM000666.1:g.187118317_187118318insT	GRCh37
NC_000004.10:g.187355311_187355312insT	NCBI36
NG_007965.1:g.10644_10645insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.604+33_604+34insT MANE Select	ENSP00000368079.4:n.604+33_604+34insT
ENST00000378802.4:c.604+33_604+34insT	ENSP00000368079.4:n.604+33_604+34insT
ENST00000507209.5:n.1076_1077insT
NM_207352.3:c.604+33_604+34insT	NP_997235.3:n.604+33_604+34insT
XM_005262935.2:c.604+33_604+34insT	XP_005262992.1:n.604+33_604+34insT
XM_006714184.2:c.208+33_208+34insT	XP_006714247.1:n.208+33_208+34insT
XM_005262935.4:c.604+33_604+34insT	XP_005262992.1:n.604+33_604+34insT
XM_017008037.1:c.208+33_208+34insT	XP_016863526.1:n.208+33_208+34insT
NM_207352.4:c.604+33_604+34insT MANE Select	NP_997235.3:n.604+33_604+34insT