Canonical Allele Identifier: CA1519888465

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204741_186204744delinsGGTT , CM000666.2:g.186204741_186204744delinsGGTT	GRCh38
NC_000004.11:g.187125895_187125898delinsGGTT , CM000666.1:g.187125895_187125898delinsGGTT	GRCh37
NC_000004.10:g.187362889_187362892delinsGGTT	NCBI36
NG_007965.1:g.18222_18225delinsGGTT
NG_012095.2:g.763_766delinsGGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-459_988-456delinsGGTT MANE Select	ENSP00000368079.4:n.988-459_988-456delinsGGTT
ENST00000378802.4:c.988-459_988-456delinsGGTT	ENSP00000368079.4:n.988-459_988-456delinsGGTT
ENST00000507209.5:n.5227_5230delinsGGTT
ENST00000513354.5:n.77+284_77+287delinsGGTT
NM_207352.3:c.988-459_988-456delinsGGTT	NP_997235.3:n.988-459_988-456delinsGGTT
XM_005262935.2:c.988-459_988-456delinsGGTT	XP_005262992.1:n.988-459_988-456delinsGGTT
XM_006714184.2:c.592-459_592-456delinsGGTT	XP_006714247.1:n.592-459_592-456delinsGGTT
XM_005262935.4:c.988-459_988-456delinsGGTT	XP_005262992.1:n.988-459_988-456delinsGGTT
XM_017008037.1:c.592-459_592-456delinsGGTT	XP_016863526.1:n.592-459_592-456delinsGGTT
NM_207352.4:c.988-459_988-456delinsGGTT MANE Select	NP_997235.3:n.988-459_988-456delinsGGTT