Canonical Allele Identifier: CA358949531

Gene: CYP4V2

Linked Data

• MyVariant Identifiers: chr4:g.187126453T>A (hg19) ; chr4:g.186205299T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205299T>A , CM000666.2:g.186205299T>A	GRCh38
NC_000004.11:g.187126453T>A , CM000666.1:g.187126453T>A	GRCh37
NC_000004.10:g.187363447T>A	NCBI36
NG_007965.1:g.18780T>A
NG_012095.2:g.1321T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1087T>A MANE Select	ENSP00000368079.4:p.Phe363Ile
ENST00000378802.4:c.1087T>A	ENSP00000368079.4:p.Phe363Ile
ENST00000502665.1:n.322T>A
ENST00000507209.5:n.5785T>A
ENST00000513354.5:n.177T>A
NM_207352.3:c.1087T>A	NP_997235.3:p.Phe363Ile
XM_005262935.2:c.1087T>A	XP_005262992.1:p.Phe363Ile
XM_006714184.2:c.691T>A	XP_006714247.1:p.Phe231Ile
XM_005262935.4:c.1087T>A	XP_005262992.1:p.Phe363Ile
XM_017008037.1:c.691T>A	XP_016863526.1:p.Phe231Ile
NM_207352.4:c.1087T>A MANE Select	NP_997235.3:p.Phe363Ile