Canonical Allele Identifier: CA2573049360

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205396_186205397delinsTC , CM000666.2:g.186205396_186205397delinsTC	GRCh38
NC_000004.11:g.187126550_187126551delinsTC , CM000666.1:g.187126550_187126551delinsTC	GRCh37
NC_000004.10:g.187363544_187363545delinsTC	NCBI36
NG_007965.1:g.18877_18878delinsTC
NG_012095.2:g.1418_1419delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+94_1090+95delinsTC MANE Select	ENSP00000368079.4:n.1090+94_1090+95delinsTC
ENST00000378802.4:c.1090+94_1090+95delinsTC	ENSP00000368079.4:n.1090+94_1090+95delinsTC
ENST00000502665.1:n.325+94_325+95delinsTC
ENST00000507209.5:n.5788+94_5788+95delinsTC
ENST00000513354.5:n.180+94_180+95delinsTC
NM_207352.3:c.1090+94_1090+95delinsTC	NP_997235.3:n.1090+94_1090+95delinsTC
XM_005262935.2:c.1090+94_1090+95delinsTC	XP_005262992.1:n.1090+94_1090+95delinsTC
XM_006714184.2:c.694+94_694+95delinsTC	XP_006714247.1:n.694+94_694+95delinsTC
XM_005262935.4:c.1090+94_1090+95delinsTC	XP_005262992.1:n.1090+94_1090+95delinsTC
XM_017008037.1:c.694+94_694+95delinsTC	XP_016863526.1:n.694+94_694+95delinsTC
NM_207352.4:c.1090+94_1090+95delinsTC MANE Select	NP_997235.3:n.1090+94_1090+95delinsTC