Canonical Allele Identifier: CA2672897003

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186205370-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205370_186205371insC , CM000666.2:g.186205370_186205371insC	GRCh38
NC_000004.11:g.187126524_187126525insC , CM000666.1:g.187126524_187126525insC	GRCh37
NC_000004.10:g.187363518_187363519insC	NCBI36
NG_007965.1:g.18851_18852insC
NG_012095.2:g.1392_1393insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+68_1090+69insC MANE Select	ENSP00000368079.4:n.1090+68_1090+69insC
ENST00000378802.4:c.1090+68_1090+69insC	ENSP00000368079.4:n.1090+68_1090+69insC
ENST00000502665.1:n.325+68_325+69insC
ENST00000507209.5:n.5788+68_5788+69insC
ENST00000513354.5:n.180+68_180+69insC
NM_207352.3:c.1090+68_1090+69insC	NP_997235.3:n.1090+68_1090+69insC
XM_005262935.2:c.1090+68_1090+69insC	XP_005262992.1:n.1090+68_1090+69insC
XM_006714184.2:c.694+68_694+69insC	XP_006714247.1:n.694+68_694+69insC
XM_005262935.4:c.1090+68_1090+69insC	XP_005262992.1:n.1090+68_1090+69insC
XM_017008037.1:c.694+68_694+69insC	XP_016863526.1:n.694+68_694+69insC
NM_207352.4:c.1090+68_1090+69insC MANE Select	NP_997235.3:n.1090+68_1090+69insC