Canonical Allele Identifier: CA2764867779

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204719_186204723del , CM000666.2:g.186204719_186204723del	GRCh38
NC_000004.11:g.187125873_187125877del , CM000666.1:g.187125873_187125877del	GRCh37
NC_000004.10:g.187362867_187362871del	NCBI36
NG_007965.1:g.18200_18204del
NG_012095.2:g.741_745del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-481_988-477del MANE Select	ENSP00000368079.4:n.988-481_988-477del
ENST00000378802.4:c.988-481_988-477del	ENSP00000368079.4:n.988-481_988-477del
ENST00000507209.5:n.5205_5209del
ENST00000513354.5:n.77+262_77+266del
NM_207352.3:c.988-481_988-477del	NP_997235.3:n.988-481_988-477del
XM_005262935.2:c.988-481_988-477del	XP_005262992.1:n.988-481_988-477del
XM_006714184.2:c.592-481_592-477del	XP_006714247.1:n.592-481_592-477del
XM_005262935.4:c.988-481_988-477del	XP_005262992.1:n.988-481_988-477del
XM_017008037.1:c.592-481_592-477del	XP_016863526.1:n.592-481_592-477del
NM_207352.4:c.988-481_988-477del MANE Select	NP_997235.3:n.988-481_988-477del