Canonical Allele Identifier: CA2764868016

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197730_186197731insT , CM000666.2:g.186197730_186197731insT	GRCh38
NC_000004.11:g.187118884_187118885insT , CM000666.1:g.187118884_187118885insT	GRCh37
NC_000004.10:g.187355878_187355879insT	NCBI36
NG_007965.1:g.11211_11212insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+128_674+129insT MANE Select	ENSP00000368079.4:n.674+128_674+129insT
ENST00000378802.4:c.674+128_674+129insT	ENSP00000368079.4:n.674+128_674+129insT
ENST00000507209.5:n.1515+128_1515+129insT
NM_207352.3:c.674+128_674+129insT	NP_997235.3:n.674+128_674+129insT
XM_005262935.2:c.674+128_674+129insT	XP_005262992.1:n.674+128_674+129insT
XM_006714184.2:c.278+128_278+129insT	XP_006714247.1:n.278+128_278+129insT
XM_005262935.4:c.674+128_674+129insT	XP_005262992.1:n.674+128_674+129insT
XM_017008037.1:c.278+128_278+129insT	XP_016863526.1:n.278+128_278+129insT
NM_207352.4:c.674+128_674+129insT MANE Select	NP_997235.3:n.674+128_674+129insT