Canonical Allele Identifier: CA2764868278

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205499_186205500insACT , CM000666.2:g.186205499_186205500insACT	GRCh38
NC_000004.11:g.187126653_187126654insACT , CM000666.1:g.187126653_187126654insACT	GRCh37
NC_000004.10:g.187363647_187363648insACT	NCBI36
NG_007965.1:g.18980_18981insACT
NG_012095.2:g.1521_1522insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+197_1090+198insACT MANE Select	ENSP00000368079.4:n.1090+197_1090+198insACT
ENST00000378802.4:c.1090+197_1090+198insACT	ENSP00000368079.4:n.1090+197_1090+198insACT
ENST00000502665.1:n.325+197_325+198insACT
ENST00000507209.5:n.5788+197_5788+198insACT
ENST00000513354.5:n.180+197_180+198insACT
NM_207352.3:c.1090+197_1090+198insACT	NP_997235.3:n.1090+197_1090+198insACT
XM_005262935.2:c.1090+197_1090+198insACT	XP_005262992.1:n.1090+197_1090+198insACT
XM_006714184.2:c.694+197_694+198insACT	XP_006714247.1:n.694+197_694+198insACT
XM_005262935.4:c.1090+197_1090+198insACT	XP_005262992.1:n.1090+197_1090+198insACT
XM_017008037.1:c.694+197_694+198insACT	XP_016863526.1:n.694+197_694+198insACT
NM_207352.4:c.1090+197_1090+198insACT MANE Select	NP_997235.3:n.1090+197_1090+198insACT