Canonical Allele Identifier: CA1519884123

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200962_186200963delinsTA , CM000666.2:g.186200962_186200963delinsTA	GRCh38
NC_000004.11:g.187122116_187122117delinsTA , CM000666.1:g.187122116_187122117delinsTA	GRCh37
NC_000004.10:g.187359110_187359111delinsTA	NCBI36
NG_007965.1:g.14443_14444delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-195_802-194delinsTA MANE Select	ENSP00000368079.4:n.802-195_802-194delinsTA
ENST00000378802.4:c.802-195_802-194delinsTA	ENSP00000368079.4:n.802-195_802-194delinsTA
ENST00000507209.5:n.1643-195_1643-194delinsTA
NM_207352.3:c.802-195_802-194delinsTA	NP_997235.3:n.802-195_802-194delinsTA
XM_005262935.2:c.802-195_802-194delinsTA	XP_005262992.1:n.802-195_802-194delinsTA
XM_006714184.2:c.406-195_406-194delinsTA	XP_006714247.1:n.406-195_406-194delinsTA
XM_005262935.4:c.802-195_802-194delinsTA	XP_005262992.1:n.802-195_802-194delinsTA
XM_017008037.1:c.406-195_406-194delinsTA	XP_016863526.1:n.406-195_406-194delinsTA
NM_207352.4:c.802-195_802-194delinsTA MANE Select	NP_997235.3:n.802-195_802-194delinsTA