Canonical Allele Identifier: CA2764868159

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205411_186205412insAGA , CM000666.2:g.186205411_186205412insAGA	GRCh38
NC_000004.11:g.187126565_187126566insAGA , CM000666.1:g.187126565_187126566insAGA	GRCh37
NC_000004.10:g.187363559_187363560insAGA	NCBI36
NG_007965.1:g.18892_18893insAGA
NG_012095.2:g.1433_1434insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+109_1090+110insAGA MANE Select	ENSP00000368079.4:n.1090+109_1090+110insAGA
ENST00000378802.4:c.1090+109_1090+110insAGA	ENSP00000368079.4:n.1090+109_1090+110insAGA
ENST00000502665.1:n.325+109_325+110insAGA
ENST00000507209.5:n.5788+109_5788+110insAGA
ENST00000513354.5:n.180+109_180+110insAGA
NM_207352.3:c.1090+109_1090+110insAGA	NP_997235.3:n.1090+109_1090+110insAGA
XM_005262935.2:c.1090+109_1090+110insAGA	XP_005262992.1:n.1090+109_1090+110insAGA
XM_006714184.2:c.694+109_694+110insAGA	XP_006714247.1:n.694+109_694+110insAGA
XM_005262935.4:c.1090+109_1090+110insAGA	XP_005262992.1:n.1090+109_1090+110insAGA
XM_017008037.1:c.694+109_694+110insAGA	XP_016863526.1:n.694+109_694+110insAGA
NM_207352.4:c.1090+109_1090+110insAGA MANE Select	NP_997235.3:n.1090+109_1090+110insAGA