Canonical Allele Identifier: CA1519883841

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736279081

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200627_186200628insAGCACTGCGA , CM000666.2:g.186200627_186200628insAGCACTGCGA	GRCh38
NC_000004.11:g.187121781_187121782insAGCACTGCGA , CM000666.1:g.187121781_187121782insAGCACTGCGA	GRCh37
NC_000004.10:g.187358775_187358776insAGCACTGCGA	NCBI36
NG_007965.1:g.14108_14109insAGCACTGCGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-530_802-529insAGCACTGCGA MANE Select	ENSP00000368079.4:n.802-530_802-529insAGCACTGCGA
ENST00000378802.4:c.802-530_802-529insAGCACTGCGA	ENSP00000368079.4:n.802-530_802-529insAGCACTGCGA
ENST00000507209.5:n.1643-530_1643-529insAGCACTGCGA
NM_207352.3:c.802-530_802-529insAGCACTGCGA	NP_997235.3:n.802-530_802-529insAGCACTGCGA
XM_005262935.2:c.802-530_802-529insAGCACTGCGA	XP_005262992.1:n.802-530_802-529insAGCACTGCGA
XM_006714184.2:c.406-530_406-529insAGCACTGCGA	XP_006714247.1:n.406-530_406-529insAGCACTGCGA
XM_005262935.4:c.802-530_802-529insAGCACTGCGA	XP_005262992.1:n.802-530_802-529insAGCACTGCGA
XM_017008037.1:c.406-530_406-529insAGCACTGCGA	XP_016863526.1:n.406-530_406-529insAGCACTGCGA
NM_207352.4:c.802-530_802-529insAGCACTGCGA MANE Select	NP_997235.3:n.802-530_802-529insAGCACTGCGA