Canonical Allele Identifier: CA2764867938

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197664_186197665insACT , CM000666.2:g.186197664_186197665insACT	GRCh38
NC_000004.11:g.187118818_187118819insACT , CM000666.1:g.187118818_187118819insACT	GRCh37
NC_000004.10:g.187355812_187355813insACT	NCBI36
NG_007965.1:g.11145_11146insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+62_674+63insACT MANE Select	ENSP00000368079.4:n.674+62_674+63insACT
ENST00000378802.4:c.674+62_674+63insACT	ENSP00000368079.4:n.674+62_674+63insACT
ENST00000507209.5:n.1515+62_1515+63insACT
NM_207352.3:c.674+62_674+63insACT	NP_997235.3:n.674+62_674+63insACT
XM_005262935.2:c.674+62_674+63insACT	XP_005262992.1:n.674+62_674+63insACT
XM_006714184.2:c.278+62_278+63insACT	XP_006714247.1:n.278+62_278+63insACT
XM_005262935.4:c.674+62_674+63insACT	XP_005262992.1:n.674+62_674+63insACT
XM_017008037.1:c.278+62_278+63insACT	XP_016863526.1:n.278+62_278+63insACT
NM_207352.4:c.674+62_674+63insACT MANE Select	NP_997235.3:n.674+62_674+63insACT