Canonical Allele Identifier: CA2764868035

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197739dup , CM000666.2:g.186197739dup	GRCh38
NC_000004.11:g.187118893dup , CM000666.1:g.187118893dup	GRCh37
NC_000004.10:g.187355887dup	NCBI36
NG_007965.1:g.11220dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+137dup MANE Select	ENSP00000368079.4:n.674+137dup
ENST00000378802.4:c.674+137dup	ENSP00000368079.4:n.674+137dup
ENST00000507209.5:n.1515+137dup
NM_207352.3:c.674+137dup	NP_997235.3:n.674+137dup
XM_005262935.2:c.674+137dup	XP_005262992.1:n.674+137dup
XM_006714184.2:c.278+137dup	XP_006714247.1:n.278+137dup
XM_005262935.4:c.674+137dup	XP_005262992.1:n.674+137dup
XM_017008037.1:c.278+137dup	XP_016863526.1:n.278+137dup
NM_207352.4:c.674+137dup MANE Select	NP_997235.3:n.674+137dup