Canonical Allele Identifier: CA2672896851

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186205137-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205139del , CM000666.2:g.186205139del	GRCh38
NC_000004.11:g.187126293del , CM000666.1:g.187126293del	GRCh37
NC_000004.10:g.187363287del	NCBI36
NG_007965.1:g.18620del
NG_012095.2:g.1161del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-61del MANE Select	ENSP00000368079.4:n.988-61del
ENST00000378802.4:c.988-61del	ENSP00000368079.4:n.988-61del
ENST00000502665.1:n.223-61del
ENST00000507209.5:n.5625del
ENST00000513354.5:n.78-61del
NM_207352.3:c.988-61del	NP_997235.3:n.988-61del
XM_005262935.2:c.988-61del	XP_005262992.1:n.988-61del
XM_006714184.2:c.592-61del	XP_006714247.1:n.592-61del
XM_005262935.4:c.988-61del	XP_005262992.1:n.988-61del
XM_017008037.1:c.592-61del	XP_016863526.1:n.592-61del
NM_207352.4:c.988-61del MANE Select	NP_997235.3:n.988-61del