Canonical Allele Identifier: CA1519918820

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197222_186197223delinsGA , CM000666.2:g.186197222_186197223delinsGA	GRCh38
NC_000004.11:g.187118376_187118377delinsGA , CM000666.1:g.187118376_187118377delinsGA	GRCh37
NC_000004.10:g.187355370_187355371delinsGA	NCBI36
NG_007965.1:g.10703_10704delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.604+92_604+93delinsGA MANE Select	ENSP00000368079.4:n.604+92_604+93delinsGA
ENST00000378802.4:c.604+92_604+93delinsGA	ENSP00000368079.4:n.604+92_604+93delinsGA
ENST00000507209.5:n.1135_1136delinsGA
NM_207352.3:c.604+92_604+93delinsGA	NP_997235.3:n.604+92_604+93delinsGA
XM_005262935.2:c.604+92_604+93delinsGA	XP_005262992.1:n.604+92_604+93delinsGA
XM_006714184.2:c.208+92_208+93delinsGA	XP_006714247.1:n.208+92_208+93delinsGA
XM_005262935.4:c.604+92_604+93delinsGA	XP_005262992.1:n.604+92_604+93delinsGA
XM_017008037.1:c.208+92_208+93delinsGA	XP_016863526.1:n.208+92_208+93delinsGA
NM_207352.4:c.604+92_604+93delinsGA MANE Select	NP_997235.3:n.604+92_604+93delinsGA