Canonical Allele Identifier: CA2764867962

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205332_186205333insAC , CM000666.2:g.186205332_186205333insAC	GRCh38
NC_000004.11:g.187126486_187126487insAC , CM000666.1:g.187126486_187126487insAC	GRCh37
NC_000004.10:g.187363480_187363481insAC	NCBI36
NG_007965.1:g.18813_18814insAC
NG_012095.2:g.1354_1355insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+30_1090+31insAC MANE Select	ENSP00000368079.4:n.1090+30_1090+31insAC
ENST00000378802.4:c.1090+30_1090+31insAC	ENSP00000368079.4:n.1090+30_1090+31insAC
ENST00000502665.1:n.325+30_325+31insAC
ENST00000507209.5:n.5788+30_5788+31insAC
ENST00000513354.5:n.180+30_180+31insAC
NM_207352.3:c.1090+30_1090+31insAC	NP_997235.3:n.1090+30_1090+31insAC
XM_005262935.2:c.1090+30_1090+31insAC	XP_005262992.1:n.1090+30_1090+31insAC
XM_006714184.2:c.694+30_694+31insAC	XP_006714247.1:n.694+30_694+31insAC
XM_005262935.4:c.1090+30_1090+31insAC	XP_005262992.1:n.1090+30_1090+31insAC
XM_017008037.1:c.694+30_694+31insAC	XP_016863526.1:n.694+30_694+31insAC
NM_207352.4:c.1090+30_1090+31insAC MANE Select	NP_997235.3:n.1090+30_1090+31insAC