Canonical Allele Identifier: CA2764867971

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197697_186197698insAG , CM000666.2:g.186197697_186197698insAG	GRCh38
NC_000004.11:g.187118851_187118852insAG , CM000666.1:g.187118851_187118852insAG	GRCh37
NC_000004.10:g.187355845_187355846insAG	NCBI36
NG_007965.1:g.11178_11179insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+95_674+96insAG MANE Select	ENSP00000368079.4:n.674+95_674+96insAG
ENST00000378802.4:c.674+95_674+96insAG	ENSP00000368079.4:n.674+95_674+96insAG
ENST00000507209.5:n.1515+95_1515+96insAG
NM_207352.3:c.674+95_674+96insAG	NP_997235.3:n.674+95_674+96insAG
XM_005262935.2:c.674+95_674+96insAG	XP_005262992.1:n.674+95_674+96insAG
XM_006714184.2:c.278+95_278+96insAG	XP_006714247.1:n.278+95_278+96insAG
XM_005262935.4:c.674+95_674+96insAG	XP_005262992.1:n.674+95_674+96insAG
XM_017008037.1:c.278+95_278+96insAG	XP_016863526.1:n.278+95_278+96insAG
NM_207352.4:c.674+95_674+96insAG MANE Select	NP_997235.3:n.674+95_674+96insAG