Canonical Allele Identifier: CA163151098

Gene: CYP3A4

Linked Data

• dbSNP Id: rs72552795
• MyVariant Identifiers: chr7:g.99358465_99358466insG (hg19) ; chr7:g.99760842_99760843insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760844dup , CM000669.2:g.99760844dup	GRCh38
NC_000007.13:g.99358467dup , CM000669.1:g.99358467dup	GRCh37
NC_000007.12:g.99196403dup	NCBI36
NG_008421.1:g.28343dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1485dup	ENSP00000337915.3:p.Phe496LeufsTer5
ENST00000651162.1:n.827dup
ENST00000651514.1:c.1392dup MANE Select	ENSP00000498939.1:p.Phe465LeufsTer5
ENST00000651783.1:c.933dup	ENSP00000498924.1:p.Phe312LeufsTer5
ENST00000652018.1:c.1245dup	ENSP00000498733.1:p.Phe416LeufsTer5
ENST00000336411.6:c.1392dup	ENSP00000337915.2:p.Phe465LeufsTer5
ENST00000354593.6:c.942dup	ENSP00000346607.2:p.Phe315LeufsTer5
NM_001202855.2:c.1389dup	NP_001189784.1:p.Phe464LeufsTer5
NM_017460.5:c.1392dup	NP_059488.2:p.Phe465LeufsTer5
XM_011515841.1:c.1485dup	XP_011514143.1:p.Phe496LeufsTer5
XM_011515842.1:c.1482dup	XP_011514144.1:p.Phe495LeufsTer5
NM_017460.6:c.1392dup MANE Select	NP_059488.2:p.Phe465LeufsTer5
NM_001202855.3:c.1389dup	NP_001189784.1:p.Phe464LeufsTer5