Canonical Allele Identifier: CA1519891211

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208737_186208740delinsGTTC , CM000666.2:g.186208737_186208740delinsGTTC	GRCh38
NC_000004.11:g.187129891_187129894delinsGTTC , CM000666.1:g.187129891_187129894delinsGTTC	GRCh37
NC_000004.10:g.187366885_187366888delinsGTTC	NCBI36
NG_007965.1:g.22218_22221delinsGTTC
NG_012095.2:g.4759_4762delinsGTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1091-128_1091-125delinsGTTC MANE Select	ENSP00000368079.4:n.1091-128_1091-125delinsGTTC
ENST00000378802.4:c.1091-128_1091-125delinsGTTC	ENSP00000368079.4:n.1091-128_1091-125delinsGTTC
ENST00000502665.1:n.326-128_326-125delinsGTTC
ENST00000507209.5:n.5789-128_5789-125delinsGTTC
ENST00000513354.5:n.181-128_181-125delinsGTTC
NM_207352.3:c.1091-128_1091-125delinsGTTC	NP_997235.3:n.1091-128_1091-125delinsGTTC
XM_005262935.2:c.1091-128_1091-125delinsGTTC	XP_005262992.1:n.1091-128_1091-125delinsGTTC
XM_006714184.2:c.695-128_695-125delinsGTTC	XP_006714247.1:n.695-128_695-125delinsGTTC
XM_005262935.4:c.1091-128_1091-125delinsGTTC	XP_005262992.1:n.1091-128_1091-125delinsGTTC
XM_017008037.1:c.695-128_695-125delinsGTTC	XP_016863526.1:n.695-128_695-125delinsGTTC
NM_207352.4:c.1091-128_1091-125delinsGTTC MANE Select	NP_997235.3:n.1091-128_1091-125delinsGTTC