Canonical Allele Identifier: CA368367581

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358461T>A (hg19) ; chr7:g.99760838T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760838T>A , CM000669.2:g.99760838T>A	GRCh38
NC_000007.13:g.99358461T>A , CM000669.1:g.99358461T>A	GRCh37
NC_000007.12:g.99196397T>A	NCBI36
NG_008421.1:g.28348A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1490A>T	ENSP00000337915.3:p.Lys497Ile
ENST00000651162.1:n.832A>T
ENST00000651514.1:c.1397A>T MANE Select	ENSP00000498939.1:p.Lys466Ile
ENST00000651783.1:c.938A>T	ENSP00000498924.1:p.Lys313Ile
ENST00000652018.1:c.1250A>T	ENSP00000498733.1:p.Lys417Ile
ENST00000336411.6:c.1397A>T	ENSP00000337915.2:p.Lys466Ile
ENST00000354593.6:c.947A>T	ENSP00000346607.2:p.Lys316Ile
NM_001202855.2:c.1394A>T	NP_001189784.1:p.Lys465Ile
NM_017460.5:c.1397A>T	NP_059488.2:p.Lys466Ile
XM_011515841.1:c.1490A>T	XP_011514143.1:p.Lys497Ile
XM_011515842.1:c.1487A>T	XP_011514144.1:p.Lys496Ile
NM_017460.6:c.1397A>T MANE Select	NP_059488.2:p.Lys466Ile
NM_001202855.3:c.1394A>T	NP_001189784.1:p.Lys465Ile