Canonical Allele Identifier: CA2764867960

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197693_186197698del , CM000666.2:g.186197693_186197698del	GRCh38
NC_000004.11:g.187118847_187118852del , CM000666.1:g.187118847_187118852del	GRCh37
NC_000004.10:g.187355841_187355846del	NCBI36
NG_007965.1:g.11174_11179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+91_674+96del MANE Select	ENSP00000368079.4:n.674+91_674+96del
ENST00000378802.4:c.674+91_674+96del	ENSP00000368079.4:n.674+91_674+96del
ENST00000507209.5:n.1515+91_1515+96del
NM_207352.3:c.674+91_674+96del	NP_997235.3:n.674+91_674+96del
XM_005262935.2:c.674+91_674+96del	XP_005262992.1:n.674+91_674+96del
XM_006714184.2:c.278+91_278+96del	XP_006714247.1:n.278+91_278+96del
XM_005262935.4:c.674+91_674+96del	XP_005262992.1:n.674+91_674+96del
XM_017008037.1:c.278+91_278+96del	XP_016863526.1:n.278+91_278+96del
NM_207352.4:c.674+91_674+96del MANE Select	NP_997235.3:n.674+91_674+96del