Canonical Allele Identifier: CA2764868276

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205496_186205497insTC , CM000666.2:g.186205496_186205497insTC	GRCh38
NC_000004.11:g.187126650_187126651insTC , CM000666.1:g.187126650_187126651insTC	GRCh37
NC_000004.10:g.187363644_187363645insTC	NCBI36
NG_007965.1:g.18977_18978insTC
NG_012095.2:g.1518_1519insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+194_1090+195insTC MANE Select	ENSP00000368079.4:n.1090+194_1090+195insTC
ENST00000378802.4:c.1090+194_1090+195insTC	ENSP00000368079.4:n.1090+194_1090+195insTC
ENST00000502665.1:n.325+194_325+195insTC
ENST00000507209.5:n.5788+194_5788+195insTC
ENST00000513354.5:n.180+194_180+195insTC
NM_207352.3:c.1090+194_1090+195insTC	NP_997235.3:n.1090+194_1090+195insTC
XM_005262935.2:c.1090+194_1090+195insTC	XP_005262992.1:n.1090+194_1090+195insTC
XM_006714184.2:c.694+194_694+195insTC	XP_006714247.1:n.694+194_694+195insTC
XM_005262935.4:c.1090+194_1090+195insTC	XP_005262992.1:n.1090+194_1090+195insTC
XM_017008037.1:c.694+194_694+195insTC	XP_016863526.1:n.694+194_694+195insTC
NM_207352.4:c.1090+194_1090+195insTC MANE Select	NP_997235.3:n.1090+194_1090+195insTC