Canonical Allele Identifier: CA2672897258

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186197254-TTCTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197255_186197258del , CM000666.2:g.186197255_186197258del	GRCh38
NC_000004.11:g.187118409_187118412del , CM000666.1:g.187118409_187118412del	GRCh37
NC_000004.10:g.187355403_187355406del	NCBI36
NG_007965.1:g.10736_10739del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.604+125_604+128del MANE Select	ENSP00000368079.4:n.604+125_604+128del
ENST00000378802.4:c.604+125_604+128del	ENSP00000368079.4:n.604+125_604+128del
ENST00000507209.5:n.1168_1171del
NM_207352.3:c.604+125_604+128del	NP_997235.3:n.604+125_604+128del
XM_005262935.2:c.604+125_604+128del	XP_005262992.1:n.604+125_604+128del
XM_006714184.2:c.208+125_208+128del	XP_006714247.1:n.208+125_208+128del
XM_005262935.4:c.604+125_604+128del	XP_005262992.1:n.604+125_604+128del
XM_017008037.1:c.208+125_208+128del	XP_016863526.1:n.208+125_208+128del
NM_207352.4:c.604+125_604+128del MANE Select	NP_997235.3:n.604+125_604+128del