Canonical Allele Identifier: CA2764867784

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204722_186204723insAGA , CM000666.2:g.186204722_186204723insAGA	GRCh38
NC_000004.11:g.187125876_187125877insAGA , CM000666.1:g.187125876_187125877insAGA	GRCh37
NC_000004.10:g.187362870_187362871insAGA	NCBI36
NG_007965.1:g.18203_18204insAGA
NG_012095.2:g.744_745insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-478_988-477insAGA MANE Select	ENSP00000368079.4:n.988-478_988-477insAGA
ENST00000378802.4:c.988-478_988-477insAGA	ENSP00000368079.4:n.988-478_988-477insAGA
ENST00000507209.5:n.5208_5209insAGA
ENST00000513354.5:n.77+265_77+266insAGA
NM_207352.3:c.988-478_988-477insAGA	NP_997235.3:n.988-478_988-477insAGA
XM_005262935.2:c.988-478_988-477insAGA	XP_005262992.1:n.988-478_988-477insAGA
XM_006714184.2:c.592-478_592-477insAGA	XP_006714247.1:n.592-478_592-477insAGA
XM_005262935.4:c.988-478_988-477insAGA	XP_005262992.1:n.988-478_988-477insAGA
XM_017008037.1:c.592-478_592-477insAGA	XP_016863526.1:n.592-478_592-477insAGA
NM_207352.4:c.988-478_988-477insAGA MANE Select	NP_997235.3:n.988-478_988-477insAGA