Canonical Allele Identifier: CA2764867754

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204702_186204703insAGAT , CM000666.2:g.186204702_186204703insAGAT	GRCh38
NC_000004.11:g.187125856_187125857insAGAT , CM000666.1:g.187125856_187125857insAGAT	GRCh37
NC_000004.10:g.187362850_187362851insAGAT	NCBI36
NG_007965.1:g.18183_18184insAGAT
NG_012095.2:g.724_725insAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-498_988-497insAGAT MANE Select	ENSP00000368079.4:n.988-498_988-497insAGAT
ENST00000378802.4:c.988-498_988-497insAGAT	ENSP00000368079.4:n.988-498_988-497insAGAT
ENST00000507209.5:n.5188_5189insAGAT
ENST00000513354.5:n.77+245_77+246insAGAT
NM_207352.3:c.988-498_988-497insAGAT	NP_997235.3:n.988-498_988-497insAGAT
XM_005262935.2:c.988-498_988-497insAGAT	XP_005262992.1:n.988-498_988-497insAGAT
XM_006714184.2:c.592-498_592-497insAGAT	XP_006714247.1:n.592-498_592-497insAGAT
XM_005262935.4:c.988-498_988-497insAGAT	XP_005262992.1:n.988-498_988-497insAGAT
XM_017008037.1:c.592-498_592-497insAGAT	XP_016863526.1:n.592-498_592-497insAGAT
NM_207352.4:c.988-498_988-497insAGAT MANE Select	NP_997235.3:n.988-498_988-497insAGAT