Canonical Allele Identifier: CA1519891212

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736607114
• gnomAD v4: 4-186208737-GTTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208743_186208745del , CM000666.2:g.186208743_186208745del	GRCh38
NC_000004.11:g.187129897_187129899del , CM000666.1:g.187129897_187129899del	GRCh37
NC_000004.10:g.187366891_187366893del	NCBI36
NG_007965.1:g.22224_22226del
NG_012095.2:g.4765_4767del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1091-122_1091-120del MANE Select	ENSP00000368079.4:n.1091-122_1091-120del
ENST00000378802.4:c.1091-122_1091-120del	ENSP00000368079.4:n.1091-122_1091-120del
ENST00000502665.1:n.326-122_326-120del
ENST00000507209.5:n.5789-122_5789-120del
ENST00000513354.5:n.181-122_181-120del
NM_207352.3:c.1091-122_1091-120del	NP_997235.3:n.1091-122_1091-120del
XM_005262935.2:c.1091-122_1091-120del	XP_005262992.1:n.1091-122_1091-120del
XM_006714184.2:c.695-122_695-120del	XP_006714247.1:n.695-122_695-120del
XM_005262935.4:c.1091-122_1091-120del	XP_005262992.1:n.1091-122_1091-120del
XM_017008037.1:c.695-122_695-120del	XP_016863526.1:n.695-122_695-120del
NM_207352.4:c.1091-122_1091-120del MANE Select	NP_997235.3:n.1091-122_1091-120del