Canonical Allele Identifier: CA2764867683

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204662_186204663insT , CM000666.2:g.186204662_186204663insT	GRCh38
NC_000004.11:g.187125816_187125817insT , CM000666.1:g.187125816_187125817insT	GRCh37
NC_000004.10:g.187362810_187362811insT	NCBI36
NG_007965.1:g.18143_18144insT
NG_012095.2:g.684_685insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-538_988-537insT MANE Select	ENSP00000368079.4:n.988-538_988-537insT
ENST00000378802.4:c.988-538_988-537insT	ENSP00000368079.4:n.988-538_988-537insT
ENST00000507209.5:n.5148_5149insT
ENST00000513354.5:n.77+205_77+206insT
NM_207352.3:c.988-538_988-537insT	NP_997235.3:n.988-538_988-537insT
XM_005262935.2:c.988-538_988-537insT	XP_005262992.1:n.988-538_988-537insT
XM_006714184.2:c.592-538_592-537insT	XP_006714247.1:n.592-538_592-537insT
XM_005262935.4:c.988-538_988-537insT	XP_005262992.1:n.988-538_988-537insT
XM_017008037.1:c.592-538_592-537insT	XP_016863526.1:n.592-538_592-537insT
NM_207352.4:c.988-538_988-537insT MANE Select	NP_997235.3:n.988-538_988-537insT