Canonical Allele Identifier: CA2764868249

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205462_186205463insAC , CM000666.2:g.186205462_186205463insAC	GRCh38
NC_000004.11:g.187126616_187126617insAC , CM000666.1:g.187126616_187126617insAC	GRCh37
NC_000004.10:g.187363610_187363611insAC	NCBI36
NG_007965.1:g.18943_18944insAC
NG_012095.2:g.1484_1485insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+160_1090+161insAC MANE Select	ENSP00000368079.4:n.1090+160_1090+161insAC
ENST00000378802.4:c.1090+160_1090+161insAC	ENSP00000368079.4:n.1090+160_1090+161insAC
ENST00000502665.1:n.325+160_325+161insAC
ENST00000507209.5:n.5788+160_5788+161insAC
ENST00000513354.5:n.180+160_180+161insAC
NM_207352.3:c.1090+160_1090+161insAC	NP_997235.3:n.1090+160_1090+161insAC
XM_005262935.2:c.1090+160_1090+161insAC	XP_005262992.1:n.1090+160_1090+161insAC
XM_006714184.2:c.694+160_694+161insAC	XP_006714247.1:n.694+160_694+161insAC
XM_005262935.4:c.1090+160_1090+161insAC	XP_005262992.1:n.1090+160_1090+161insAC
XM_017008037.1:c.694+160_694+161insAC	XP_016863526.1:n.694+160_694+161insAC
NM_207352.4:c.1090+160_1090+161insAC MANE Select	NP_997235.3:n.1090+160_1090+161insAC