Canonical Allele Identifier: CA1519883886

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736280148

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200672_186200692del , CM000666.2:g.186200672_186200692del	GRCh38
NC_000004.11:g.187121826_187121846del , CM000666.1:g.187121826_187121846del	GRCh37
NC_000004.10:g.187358820_187358840del	NCBI36
NG_007965.1:g.14153_14173del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-485_802-465del MANE Select	ENSP00000368079.4:n.802-485_802-465del
ENST00000378802.4:c.802-485_802-465del	ENSP00000368079.4:n.802-485_802-465del
ENST00000507209.5:n.1643-485_1643-465del
NM_207352.3:c.802-485_802-465del	NP_997235.3:n.802-485_802-465del
XM_005262935.2:c.802-485_802-465del	XP_005262992.1:n.802-485_802-465del
XM_006714184.2:c.406-485_406-465del	XP_006714247.1:n.406-485_406-465del
XM_005262935.4:c.802-485_802-465del	XP_005262992.1:n.802-485_802-465del
XM_017008037.1:c.406-485_406-465del	XP_016863526.1:n.406-485_406-465del
NM_207352.4:c.802-485_802-465del MANE Select	NP_997235.3:n.802-485_802-465del