Canonical Allele Identifier: CA456686437

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358463G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760840G>A , CM000669.2:g.99760840G>A	GRCh38
NC_000007.13:g.99358463G>A , CM000669.1:g.99358463G>A	GRCh37
NC_000007.12:g.99196399G>A	NCBI36
NG_008421.1:g.28346C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1488C>T	ENSP00000337915.3:p.Phe496=
ENST00000651162.1:n.830C>T
ENST00000651514.1:c.1395C>T MANE Select	ENSP00000498939.1:p.Phe465=
ENST00000651783.1:c.936C>T	ENSP00000498924.1:p.Phe312=
ENST00000652018.1:c.1248C>T	ENSP00000498733.1:p.Phe416=
ENST00000336411.6:c.1395C>T	ENSP00000337915.2:p.Phe465=
ENST00000354593.6:c.945C>T	ENSP00000346607.2:p.Phe315=
NM_001202855.2:c.1392C>T	NP_001189784.1:p.Phe464=
NM_017460.5:c.1395C>T	NP_059488.2:p.Phe465=
XM_011515841.1:c.1488C>T	XP_011514143.1:p.Phe496=
XM_011515842.1:c.1485C>T	XP_011514144.1:p.Phe495=
NM_017460.6:c.1395C>T MANE Select	NP_059488.2:p.Phe465=
NM_001202855.3:c.1392C>T	NP_001189784.1:p.Phe464=