Canonical Allele Identifier: CA2764867944

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197679_186197684del , CM000666.2:g.186197679_186197684del	GRCh38
NC_000004.11:g.187118833_187118838del , CM000666.1:g.187118833_187118838del	GRCh37
NC_000004.10:g.187355827_187355832del	NCBI36
NG_007965.1:g.11160_11165del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+77_674+82del MANE Select	ENSP00000368079.4:n.674+77_674+82del
ENST00000378802.4:c.674+77_674+82del	ENSP00000368079.4:n.674+77_674+82del
ENST00000507209.5:n.1515+77_1515+82del
NM_207352.3:c.674+77_674+82del	NP_997235.3:n.674+77_674+82del
XM_005262935.2:c.674+77_674+82del	XP_005262992.1:n.674+77_674+82del
XM_006714184.2:c.278+77_278+82del	XP_006714247.1:n.278+77_278+82del
XM_005262935.4:c.674+77_674+82del	XP_005262992.1:n.674+77_674+82del
XM_017008037.1:c.278+77_278+82del	XP_016863526.1:n.278+77_278+82del
NM_207352.4:c.674+77_674+82del MANE Select	NP_997235.3:n.674+77_674+82del