Canonical Allele Identifier: CA2672896484

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186204903-AAGGCGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204906_186204911del , CM000666.2:g.186204906_186204911del	GRCh38
NC_000004.11:g.187126060_187126065del , CM000666.1:g.187126060_187126065del	GRCh37
NC_000004.10:g.187363054_187363059del	NCBI36
NG_007965.1:g.18387_18392del
NG_012095.2:g.928_933del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-294_988-289del MANE Select	ENSP00000368079.4:n.988-294_988-289del
ENST00000378802.4:c.988-294_988-289del	ENSP00000368079.4:n.988-294_988-289del
ENST00000502665.1:n.70_75del
ENST00000507209.5:n.5392_5397del
ENST00000513354.5:n.78-294_78-289del
NM_207352.3:c.988-294_988-289del	NP_997235.3:n.988-294_988-289del
XM_005262935.2:c.988-294_988-289del	XP_005262992.1:n.988-294_988-289del
XM_006714184.2:c.592-294_592-289del	XP_006714247.1:n.592-294_592-289del
XM_005262935.4:c.988-294_988-289del	XP_005262992.1:n.988-294_988-289del
XM_017008037.1:c.592-294_592-289del	XP_016863526.1:n.592-294_592-289del
NM_207352.4:c.988-294_988-289del MANE Select	NP_997235.3:n.988-294_988-289del