Canonical Allele Identifier: CA2764868155

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205409_186205410insAGT , CM000666.2:g.186205409_186205410insAGT	GRCh38
NC_000004.11:g.187126563_187126564insAGT , CM000666.1:g.187126563_187126564insAGT	GRCh37
NC_000004.10:g.187363557_187363558insAGT	NCBI36
NG_007965.1:g.18890_18891insAGT
NG_012095.2:g.1431_1432insAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+107_1090+108insAGT MANE Select	ENSP00000368079.4:n.1090+107_1090+108insAGT
ENST00000378802.4:c.1090+107_1090+108insAGT	ENSP00000368079.4:n.1090+107_1090+108insAGT
ENST00000502665.1:n.325+107_325+108insAGT
ENST00000507209.5:n.5788+107_5788+108insAGT
ENST00000513354.5:n.180+107_180+108insAGT
NM_207352.3:c.1090+107_1090+108insAGT	NP_997235.3:n.1090+107_1090+108insAGT
XM_005262935.2:c.1090+107_1090+108insAGT	XP_005262992.1:n.1090+107_1090+108insAGT
XM_006714184.2:c.694+107_694+108insAGT	XP_006714247.1:n.694+107_694+108insAGT
XM_005262935.4:c.1090+107_1090+108insAGT	XP_005262992.1:n.1090+107_1090+108insAGT
XM_017008037.1:c.694+107_694+108insAGT	XP_016863526.1:n.694+107_694+108insAGT
NM_207352.4:c.1090+107_1090+108insAGT MANE Select	NP_997235.3:n.1090+107_1090+108insAGT