Canonical Allele Identifier: CA2764867173

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194675_186194676insTG , CM000666.2:g.186194675_186194676insTG	GRCh38
NC_000004.11:g.187115829_187115830insTG , CM000666.1:g.187115829_187115830insTG	GRCh37
NC_000004.10:g.187352823_187352824insTG	NCBI36
NG_007965.1:g.8156_8157insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.327+63_327+64insTG MANE Select	ENSP00000368079.4:n.327+63_327+64insTG
ENST00000378802.4:c.327+63_327+64insTG	ENSP00000368079.4:n.327+63_327+64insTG
NM_207352.3:c.327+63_327+64insTG	NP_997235.3:n.327+63_327+64insTG
XM_005262935.2:c.327+63_327+64insTG	XP_005262992.1:n.327+63_327+64insTG
XM_006714184.2:c.17+63_17+64insTG	XP_006714247.1:n.17+63_17+64insTG
XM_005262935.4:c.327+63_327+64insTG	XP_005262992.1:n.327+63_327+64insTG
XM_017008037.1:c.17+63_17+64insTG	XP_016863526.1:n.17+63_17+64insTG
NM_207352.4:c.327+63_327+64insTG MANE Select	NP_997235.3:n.327+63_327+64insTG