Canonical Allele Identifier: CA2764868529

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200902_186201099del , CM000666.2:g.186200902_186201099del	GRCh38
NC_000004.11:g.187122056_187122253del , CM000666.1:g.187122056_187122253del	GRCh37
NC_000004.10:g.187359050_187359247del	NCBI36
NG_007965.1:g.14383_14580del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-255_802-58del MANE Select	ENSP00000368079.4:n.802-255_802-58del
ENST00000378802.4:c.802-255_802-58del	ENSP00000368079.4:n.802-255_802-58del
ENST00000507209.5:n.1643-255_1643-58del
NM_207352.3:c.802-255_802-58del	NP_997235.3:n.802-255_802-58del
XM_005262935.2:c.802-255_802-58del	XP_005262992.1:n.802-255_802-58del
XM_006714184.2:c.406-255_406-58del	XP_006714247.1:n.406-255_406-58del
XM_005262935.4:c.802-255_802-58del	XP_005262992.1:n.802-255_802-58del
XM_017008037.1:c.406-255_406-58del	XP_016863526.1:n.406-255_406-58del
NM_207352.4:c.802-255_802-58del MANE Select	NP_997235.3:n.802-255_802-58del