Canonical Allele Identifier: CA1519915365

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194666_186194668delinsATC , CM000666.2:g.186194666_186194668delinsATC	GRCh38
NC_000004.11:g.187115820_187115822delinsATC , CM000666.1:g.187115820_187115822delinsATC	GRCh37
NC_000004.10:g.187352814_187352816delinsATC	NCBI36
NG_007965.1:g.8147_8149delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.327+54_327+56delinsATC MANE Select	ENSP00000368079.4:n.327+54_327+56delinsATC
ENST00000378802.4:c.327+54_327+56delinsATC	ENSP00000368079.4:n.327+54_327+56delinsATC
NM_207352.3:c.327+54_327+56delinsATC	NP_997235.3:n.327+54_327+56delinsATC
XM_005262935.2:c.327+54_327+56delinsATC	XP_005262992.1:n.327+54_327+56delinsATC
XM_006714184.2:c.17+54_17+56delinsATC	XP_006714247.1:n.17+54_17+56delinsATC
XM_005262935.4:c.327+54_327+56delinsATC	XP_005262992.1:n.327+54_327+56delinsATC
XM_017008037.1:c.17+54_17+56delinsATC	XP_016863526.1:n.17+54_17+56delinsATC
NM_207352.4:c.327+54_327+56delinsATC MANE Select	NP_997235.3:n.327+54_327+56delinsATC