Canonical Allele Identifier: CA2764867789

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197142_186197143insAGA , CM000666.2:g.186197142_186197143insAGA	GRCh38
NC_000004.11:g.187118296_187118297insAGA , CM000666.1:g.187118296_187118297insAGA	GRCh37
NC_000004.10:g.187355290_187355291insAGA	NCBI36
NG_007965.1:g.10623_10624insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.604+12_604+13insAGA MANE Select	ENSP00000368079.4:n.604+12_604+13insAGA
ENST00000378802.4:c.604+12_604+13insAGA	ENSP00000368079.4:n.604+12_604+13insAGA
ENST00000507209.5:n.1055_1056insAGA
NM_207352.3:c.604+12_604+13insAGA	NP_997235.3:n.604+12_604+13insAGA
XM_005262935.2:c.604+12_604+13insAGA	XP_005262992.1:n.604+12_604+13insAGA
XM_006714184.2:c.208+12_208+13insAGA	XP_006714247.1:n.208+12_208+13insAGA
XM_005262935.4:c.604+12_604+13insAGA	XP_005262992.1:n.604+12_604+13insAGA
XM_017008037.1:c.208+12_208+13insAGA	XP_016863526.1:n.208+12_208+13insAGA
NM_207352.4:c.604+12_604+13insAGA MANE Select	NP_997235.3:n.604+12_604+13insAGA