Canonical Allele Identifier: CA1519888485

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204765_186204767delinsAGG , CM000666.2:g.186204765_186204767delinsAGG	GRCh38
NC_000004.11:g.187125919_187125921delinsAGG , CM000666.1:g.187125919_187125921delinsAGG	GRCh37
NC_000004.10:g.187362913_187362915delinsAGG	NCBI36
NG_007965.1:g.18246_18248delinsAGG
NG_012095.2:g.787_789delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-435_988-433delinsAGG MANE Select	ENSP00000368079.4:n.988-435_988-433delinsAGG
ENST00000378802.4:c.988-435_988-433delinsAGG	ENSP00000368079.4:n.988-435_988-433delinsAGG
ENST00000507209.5:n.5251_5253delinsAGG
ENST00000513354.5:n.77+308_77+310delinsAGG
NM_207352.3:c.988-435_988-433delinsAGG	NP_997235.3:n.988-435_988-433delinsAGG
XM_005262935.2:c.988-435_988-433delinsAGG	XP_005262992.1:n.988-435_988-433delinsAGG
XM_006714184.2:c.592-435_592-433delinsAGG	XP_006714247.1:n.592-435_592-433delinsAGG
XM_005262935.4:c.988-435_988-433delinsAGG	XP_005262992.1:n.988-435_988-433delinsAGG
XM_017008037.1:c.592-435_592-433delinsAGG	XP_016863526.1:n.592-435_592-433delinsAGG
NM_207352.4:c.988-435_988-433delinsAGG MANE Select	NP_997235.3:n.988-435_988-433delinsAGG