Canonical Allele Identifier: CA2764868197

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205427_186205428insAG , CM000666.2:g.186205427_186205428insAG	GRCh38
NC_000004.11:g.187126581_187126582insAG , CM000666.1:g.187126581_187126582insAG	GRCh37
NC_000004.10:g.187363575_187363576insAG	NCBI36
NG_007965.1:g.18908_18909insAG
NG_012095.2:g.1449_1450insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+125_1090+126insAG MANE Select	ENSP00000368079.4:n.1090+125_1090+126insAG
ENST00000378802.4:c.1090+125_1090+126insAG	ENSP00000368079.4:n.1090+125_1090+126insAG
ENST00000502665.1:n.325+125_325+126insAG
ENST00000507209.5:n.5788+125_5788+126insAG
ENST00000513354.5:n.180+125_180+126insAG
NM_207352.3:c.1090+125_1090+126insAG	NP_997235.3:n.1090+125_1090+126insAG
XM_005262935.2:c.1090+125_1090+126insAG	XP_005262992.1:n.1090+125_1090+126insAG
XM_006714184.2:c.694+125_694+126insAG	XP_006714247.1:n.694+125_694+126insAG
XM_005262935.4:c.1090+125_1090+126insAG	XP_005262992.1:n.1090+125_1090+126insAG
XM_017008037.1:c.694+125_694+126insAG	XP_016863526.1:n.694+125_694+126insAG
NM_207352.4:c.1090+125_1090+126insAG MANE Select	NP_997235.3:n.1090+125_1090+126insAG