Canonical Allele Identifier: CA1519888486

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736445432
• gnomAD v4: 4-186204765-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204766_186204767del , CM000666.2:g.186204766_186204767del	GRCh38
NC_000004.11:g.187125920_187125921del , CM000666.1:g.187125920_187125921del	GRCh37
NC_000004.10:g.187362914_187362915del	NCBI36
NG_007965.1:g.18247_18248del
NG_012095.2:g.788_789del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-434_988-433del MANE Select	ENSP00000368079.4:n.988-434_988-433del
ENST00000378802.4:c.988-434_988-433del	ENSP00000368079.4:n.988-434_988-433del
ENST00000507209.5:n.5252_5253del
ENST00000513354.5:n.77+309_77+310del
NM_207352.3:c.988-434_988-433del	NP_997235.3:n.988-434_988-433del
XM_005262935.2:c.988-434_988-433del	XP_005262992.1:n.988-434_988-433del
XM_006714184.2:c.592-434_592-433del	XP_006714247.1:n.592-434_592-433del
XM_005262935.4:c.988-434_988-433del	XP_005262992.1:n.988-434_988-433del
XM_017008037.1:c.592-434_592-433del	XP_016863526.1:n.592-434_592-433del
NM_207352.4:c.988-434_988-433del MANE Select	NP_997235.3:n.988-434_988-433del