Canonical Allele Identifier: CA1519918795

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197216_186197219delinsTGGG , CM000666.2:g.186197216_186197219delinsTGGG	GRCh38
NC_000004.11:g.187118370_187118373delinsTGGG , CM000666.1:g.187118370_187118373delinsTGGG	GRCh37
NC_000004.10:g.187355364_187355367delinsTGGG	NCBI36
NG_007965.1:g.10697_10700delinsTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.604+86_604+89delinsTGGG MANE Select	ENSP00000368079.4:n.604+86_604+89delinsTGGG
ENST00000378802.4:c.604+86_604+89delinsTGGG	ENSP00000368079.4:n.604+86_604+89delinsTGGG
ENST00000507209.5:n.1129_1132delinsTGGG
NM_207352.3:c.604+86_604+89delinsTGGG	NP_997235.3:n.604+86_604+89delinsTGGG
XM_005262935.2:c.604+86_604+89delinsTGGG	XP_005262992.1:n.604+86_604+89delinsTGGG
XM_006714184.2:c.208+86_208+89delinsTGGG	XP_006714247.1:n.208+86_208+89delinsTGGG
XM_005262935.4:c.604+86_604+89delinsTGGG	XP_005262992.1:n.604+86_604+89delinsTGGG
XM_017008037.1:c.208+86_208+89delinsTGGG	XP_016863526.1:n.208+86_208+89delinsTGGG
NM_207352.4:c.604+86_604+89delinsTGGG MANE Select	NP_997235.3:n.604+86_604+89delinsTGGG