Canonical Allele Identifier: CA2672896828

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186205095-CAGTGCAGTCAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205096_186205106del , CM000666.2:g.186205096_186205106del	GRCh38
NC_000004.11:g.187126250_187126260del , CM000666.1:g.187126250_187126260del	GRCh37
NC_000004.10:g.187363244_187363254del	NCBI36
NG_007965.1:g.18577_18587del
NG_012095.2:g.1118_1128del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-104_988-94del MANE Select	ENSP00000368079.4:n.988-104_988-94del
ENST00000378802.4:c.988-104_988-94del	ENSP00000368079.4:n.988-104_988-94del
ENST00000502665.1:n.222+38_222+48del
ENST00000507209.5:n.5582_5592del
ENST00000513354.5:n.78-104_78-94del
NM_207352.3:c.988-104_988-94del	NP_997235.3:n.988-104_988-94del
XM_005262935.2:c.988-104_988-94del	XP_005262992.1:n.988-104_988-94del
XM_006714184.2:c.592-104_592-94del	XP_006714247.1:n.592-104_592-94del
XM_005262935.4:c.988-104_988-94del	XP_005262992.1:n.988-104_988-94del
XM_017008037.1:c.592-104_592-94del	XP_016863526.1:n.592-104_592-94del
NM_207352.4:c.988-104_988-94del MANE Select	NP_997235.3:n.988-104_988-94del