Canonical Allele Identifier: CA2764867674

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204658_186204659insACG , CM000666.2:g.186204658_186204659insACG	GRCh38
NC_000004.11:g.187125812_187125813insACG , CM000666.1:g.187125812_187125813insACG	GRCh37
NC_000004.10:g.187362806_187362807insACG	NCBI36
NG_007965.1:g.18139_18140insACG
NG_012095.2:g.680_681insACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-542_988-541insACG MANE Select	ENSP00000368079.4:n.988-542_988-541insACG
ENST00000378802.4:c.988-542_988-541insACG	ENSP00000368079.4:n.988-542_988-541insACG
ENST00000507209.5:n.5144_5145insACG
ENST00000513354.5:n.77+201_77+202insACG
NM_207352.3:c.988-542_988-541insACG	NP_997235.3:n.988-542_988-541insACG
XM_005262935.2:c.988-542_988-541insACG	XP_005262992.1:n.988-542_988-541insACG
XM_006714184.2:c.592-542_592-541insACG	XP_006714247.1:n.592-542_592-541insACG
XM_005262935.4:c.988-542_988-541insACG	XP_005262992.1:n.988-542_988-541insACG
XM_017008037.1:c.592-542_592-541insACG	XP_016863526.1:n.592-542_592-541insACG
NM_207352.4:c.988-542_988-541insACG MANE Select	NP_997235.3:n.988-542_988-541insACG