Canonical Allele Identifier: CA2764867664

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204655_186204656insCAC , CM000666.2:g.186204655_186204656insCAC	GRCh38
NC_000004.11:g.187125809_187125810insCAC , CM000666.1:g.187125809_187125810insCAC	GRCh37
NC_000004.10:g.187362803_187362804insCAC	NCBI36
NG_007965.1:g.18136_18137insCAC
NG_012095.2:g.677_678insCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-545_988-544insCAC MANE Select	ENSP00000368079.4:n.988-545_988-544insCAC
ENST00000378802.4:c.988-545_988-544insCAC	ENSP00000368079.4:n.988-545_988-544insCAC
ENST00000507209.5:n.5141_5142insCAC
ENST00000513354.5:n.77+198_77+199insCAC
NM_207352.3:c.988-545_988-544insCAC	NP_997235.3:n.988-545_988-544insCAC
XM_005262935.2:c.988-545_988-544insCAC	XP_005262992.1:n.988-545_988-544insCAC
XM_006714184.2:c.592-545_592-544insCAC	XP_006714247.1:n.592-545_592-544insCAC
XM_005262935.4:c.988-545_988-544insCAC	XP_005262992.1:n.988-545_988-544insCAC
XM_017008037.1:c.592-545_592-544insCAC	XP_016863526.1:n.592-545_592-544insCAC
NM_207352.4:c.988-545_988-544insCAC MANE Select	NP_997235.3:n.988-545_988-544insCAC