Canonical Allele Identifier: CA2672897765

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186197696-TTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197697_186197699del , CM000666.2:g.186197697_186197699del	GRCh38
NC_000004.11:g.187118851_187118853del , CM000666.1:g.187118851_187118853del	GRCh37
NC_000004.10:g.187355845_187355847del	NCBI36
NG_007965.1:g.11178_11180del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+95_674+97del MANE Select	ENSP00000368079.4:n.674+95_674+97del
ENST00000378802.4:c.674+95_674+97del	ENSP00000368079.4:n.674+95_674+97del
ENST00000507209.5:n.1515+95_1515+97del
NM_207352.3:c.674+95_674+97del	NP_997235.3:n.674+95_674+97del
XM_005262935.2:c.674+95_674+97del	XP_005262992.1:n.674+95_674+97del
XM_006714184.2:c.278+95_278+97del	XP_006714247.1:n.278+95_278+97del
XM_005262935.4:c.674+95_674+97del	XP_005262992.1:n.674+95_674+97del
XM_017008037.1:c.278+95_278+97del	XP_016863526.1:n.278+95_278+97del
NM_207352.4:c.674+95_674+97del MANE Select	NP_997235.3:n.674+95_674+97del