Canonical Allele Identifier: CA2764868192

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205425_186205426insAA , CM000666.2:g.186205425_186205426insAA	GRCh38
NC_000004.11:g.187126579_187126580insAA , CM000666.1:g.187126579_187126580insAA	GRCh37
NC_000004.10:g.187363573_187363574insAA	NCBI36
NG_007965.1:g.18906_18907insAA
NG_012095.2:g.1447_1448insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+123_1090+124insAA MANE Select	ENSP00000368079.4:n.1090+123_1090+124insAA
ENST00000378802.4:c.1090+123_1090+124insAA	ENSP00000368079.4:n.1090+123_1090+124insAA
ENST00000502665.1:n.325+123_325+124insAA
ENST00000507209.5:n.5788+123_5788+124insAA
ENST00000513354.5:n.180+123_180+124insAA
NM_207352.3:c.1090+123_1090+124insAA	NP_997235.3:n.1090+123_1090+124insAA
XM_005262935.2:c.1090+123_1090+124insAA	XP_005262992.1:n.1090+123_1090+124insAA
XM_006714184.2:c.694+123_694+124insAA	XP_006714247.1:n.694+123_694+124insAA
XM_005262935.4:c.1090+123_1090+124insAA	XP_005262992.1:n.1090+123_1090+124insAA
XM_017008037.1:c.694+123_694+124insAA	XP_016863526.1:n.694+123_694+124insAA
NM_207352.4:c.1090+123_1090+124insAA MANE Select	NP_997235.3:n.1090+123_1090+124insAA