Canonical Allele Identifier: CA2764868290

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205542_186205543insAGA , CM000666.2:g.186205542_186205543insAGA	GRCh38
NC_000004.11:g.187126696_187126697insAGA , CM000666.1:g.187126696_187126697insAGA	GRCh37
NC_000004.10:g.187363690_187363691insAGA	NCBI36
NG_007965.1:g.19023_19024insAGA
NG_012095.2:g.1564_1565insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+240_1090+241insAGA MANE Select	ENSP00000368079.4:n.1090+240_1090+241insAGA
ENST00000378802.4:c.1090+240_1090+241insAGA	ENSP00000368079.4:n.1090+240_1090+241insAGA
ENST00000502665.1:n.325+240_325+241insAGA
ENST00000507209.5:n.5788+240_5788+241insAGA
ENST00000513354.5:n.180+240_180+241insAGA
NM_207352.3:c.1090+240_1090+241insAGA	NP_997235.3:n.1090+240_1090+241insAGA
XM_005262935.2:c.1090+240_1090+241insAGA	XP_005262992.1:n.1090+240_1090+241insAGA
XM_006714184.2:c.694+240_694+241insAGA	XP_006714247.1:n.694+240_694+241insAGA
XM_005262935.4:c.1090+240_1090+241insAGA	XP_005262992.1:n.1090+240_1090+241insAGA
XM_017008037.1:c.694+240_694+241insAGA	XP_016863526.1:n.694+240_694+241insAGA
NM_207352.4:c.1090+240_1090+241insAGA MANE Select	NP_997235.3:n.1090+240_1090+241insAGA