Canonical Allele Identifier: CA2764867825

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204746_186204757del , CM000666.2:g.186204746_186204757del	GRCh38
NC_000004.11:g.187125900_187125911del , CM000666.1:g.187125900_187125911del	GRCh37
NC_000004.10:g.187362894_187362905del	NCBI36
NG_007965.1:g.18227_18238del
NG_012095.2:g.768_779del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-454_988-443del MANE Select	ENSP00000368079.4:n.988-454_988-443del
ENST00000378802.4:c.988-454_988-443del	ENSP00000368079.4:n.988-454_988-443del
ENST00000507209.5:n.5232_5243del
ENST00000513354.5:n.77+289_77+300del
NM_207352.3:c.988-454_988-443del	NP_997235.3:n.988-454_988-443del
XM_005262935.2:c.988-454_988-443del	XP_005262992.1:n.988-454_988-443del
XM_006714184.2:c.592-454_592-443del	XP_006714247.1:n.592-454_592-443del
XM_005262935.4:c.988-454_988-443del	XP_005262992.1:n.988-454_988-443del
XM_017008037.1:c.592-454_592-443del	XP_016863526.1:n.592-454_592-443del
NM_207352.4:c.988-454_988-443del MANE Select	NP_997235.3:n.988-454_988-443del