Canonical Allele Identifier: CA1519884134

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200992_186200995delinsTTAA , CM000666.2:g.186200992_186200995delinsTTAA	GRCh38
NC_000004.11:g.187122146_187122149delinsTTAA , CM000666.1:g.187122146_187122149delinsTTAA	GRCh37
NC_000004.10:g.187359140_187359143delinsTTAA	NCBI36
NG_007965.1:g.14473_14476delinsTTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-165_802-162delinsTTAA MANE Select	ENSP00000368079.4:n.802-165_802-162delinsTTAA
ENST00000378802.4:c.802-165_802-162delinsTTAA	ENSP00000368079.4:n.802-165_802-162delinsTTAA
ENST00000507209.5:n.1643-165_1643-162delinsTTAA
NM_207352.3:c.802-165_802-162delinsTTAA	NP_997235.3:n.802-165_802-162delinsTTAA
XM_005262935.2:c.802-165_802-162delinsTTAA	XP_005262992.1:n.802-165_802-162delinsTTAA
XM_006714184.2:c.406-165_406-162delinsTTAA	XP_006714247.1:n.406-165_406-162delinsTTAA
XM_005262935.4:c.802-165_802-162delinsTTAA	XP_005262992.1:n.802-165_802-162delinsTTAA
XM_017008037.1:c.406-165_406-162delinsTTAA	XP_016863526.1:n.406-165_406-162delinsTTAA
NM_207352.4:c.802-165_802-162delinsTTAA MANE Select	NP_997235.3:n.802-165_802-162delinsTTAA