Canonical Allele Identifier: CA1519891218

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208749_186208750delinsTG , CM000666.2:g.186208749_186208750delinsTG	GRCh38
NC_000004.11:g.187129903_187129904delinsTG , CM000666.1:g.187129903_187129904delinsTG	GRCh37
NC_000004.10:g.187366897_187366898delinsTG	NCBI36
NG_007965.1:g.22230_22231delinsTG
NG_012095.2:g.4771_4772delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1091-116_1091-115delinsTG MANE Select	ENSP00000368079.4:n.1091-116_1091-115delinsTG
ENST00000378802.4:c.1091-116_1091-115delinsTG	ENSP00000368079.4:n.1091-116_1091-115delinsTG
ENST00000502665.1:n.326-116_326-115delinsTG
ENST00000507209.5:n.5789-116_5789-115delinsTG
ENST00000513354.5:n.181-116_181-115delinsTG
NM_207352.3:c.1091-116_1091-115delinsTG	NP_997235.3:n.1091-116_1091-115delinsTG
XM_005262935.2:c.1091-116_1091-115delinsTG	XP_005262992.1:n.1091-116_1091-115delinsTG
XM_006714184.2:c.695-116_695-115delinsTG	XP_006714247.1:n.695-116_695-115delinsTG
XM_005262935.4:c.1091-116_1091-115delinsTG	XP_005262992.1:n.1091-116_1091-115delinsTG
XM_017008037.1:c.695-116_695-115delinsTG	XP_016863526.1:n.695-116_695-115delinsTG
NM_207352.4:c.1091-116_1091-115delinsTG MANE Select	NP_997235.3:n.1091-116_1091-115delinsTG