Canonical Allele Identifier: CA2764867658

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204648_186204649insCTG , CM000666.2:g.186204648_186204649insCTG	GRCh38
NC_000004.11:g.187125802_187125803insCTG , CM000666.1:g.187125802_187125803insCTG	GRCh37
NC_000004.10:g.187362796_187362797insCTG	NCBI36
NG_007965.1:g.18129_18130insCTG
NG_012095.2:g.670_671insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-552_988-551insCTG MANE Select	ENSP00000368079.4:n.988-552_988-551insCTG
ENST00000378802.4:c.988-552_988-551insCTG	ENSP00000368079.4:n.988-552_988-551insCTG
ENST00000507209.5:n.5134_5135insCTG
ENST00000513354.5:n.77+191_77+192insCTG
NM_207352.3:c.988-552_988-551insCTG	NP_997235.3:n.988-552_988-551insCTG
XM_005262935.2:c.988-552_988-551insCTG	XP_005262992.1:n.988-552_988-551insCTG
XM_006714184.2:c.592-552_592-551insCTG	XP_006714247.1:n.592-552_592-551insCTG
XM_005262935.4:c.988-552_988-551insCTG	XP_005262992.1:n.988-552_988-551insCTG
XM_017008037.1:c.592-552_592-551insCTG	XP_016863526.1:n.592-552_592-551insCTG
NM_207352.4:c.988-552_988-551insCTG MANE Select	NP_997235.3:n.988-552_988-551insCTG