Canonical Allele Identifier: CA1519891256

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208819_186208820delinsGC , CM000666.2:g.186208819_186208820delinsGC	GRCh38
NC_000004.11:g.187129973_187129974delinsGC , CM000666.1:g.187129973_187129974delinsGC	GRCh37
NC_000004.10:g.187366967_187366968delinsGC	NCBI36
NG_007965.1:g.22300_22301delinsGC
NG_012095.2:g.4841_4842delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1091-46_1091-45delinsGC MANE Select	ENSP00000368079.4:n.1091-46_1091-45delinsGC
ENST00000378802.4:c.1091-46_1091-45delinsGC	ENSP00000368079.4:n.1091-46_1091-45delinsGC
ENST00000502665.1:n.326-46_326-45delinsGC
ENST00000507209.5:n.5789-46_5789-45delinsGC
ENST00000513354.5:n.181-46_181-45delinsGC
NM_207352.3:c.1091-46_1091-45delinsGC	NP_997235.3:n.1091-46_1091-45delinsGC
XM_005262935.2:c.1091-46_1091-45delinsGC	XP_005262992.1:n.1091-46_1091-45delinsGC
XM_006714184.2:c.695-46_695-45delinsGC	XP_006714247.1:n.695-46_695-45delinsGC
XM_005262935.4:c.1091-46_1091-45delinsGC	XP_005262992.1:n.1091-46_1091-45delinsGC
XM_017008037.1:c.695-46_695-45delinsGC	XP_016863526.1:n.695-46_695-45delinsGC
NM_207352.4:c.1091-46_1091-45delinsGC MANE Select	NP_997235.3:n.1091-46_1091-45delinsGC