Canonical Allele Identifier: CA2764867939

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197666_186197667del , CM000666.2:g.186197666_186197667del	GRCh38
NC_000004.11:g.187118820_187118821del , CM000666.1:g.187118820_187118821del	GRCh37
NC_000004.10:g.187355814_187355815del	NCBI36
NG_007965.1:g.11147_11148del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+64_674+65del MANE Select	ENSP00000368079.4:n.674+64_674+65del
ENST00000378802.4:c.674+64_674+65del	ENSP00000368079.4:n.674+64_674+65del
ENST00000507209.5:n.1515+64_1515+65del
NM_207352.3:c.674+64_674+65del	NP_997235.3:n.674+64_674+65del
XM_005262935.2:c.674+64_674+65del	XP_005262992.1:n.674+64_674+65del
XM_006714184.2:c.278+64_278+65del	XP_006714247.1:n.278+64_278+65del
XM_005262935.4:c.674+64_674+65del	XP_005262992.1:n.674+64_674+65del
XM_017008037.1:c.278+64_278+65del	XP_016863526.1:n.278+64_278+65del
NM_207352.4:c.674+64_674+65del MANE Select	NP_997235.3:n.674+64_674+65del