Canonical Allele Identifier: CA368367642

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358473T>A (hg19) ; chr7:g.99760850T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760850T>A , CM000669.2:g.99760850T>A	GRCh38
NC_000007.13:g.99358473T>A , CM000669.1:g.99358473T>A	GRCh37
NC_000007.12:g.99196409T>A	NCBI36
NG_008421.1:g.28336A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1478A>T	ENSP00000337915.3:p.Asn493Ile
ENST00000651162.1:n.820A>T
ENST00000651514.1:c.1385A>T MANE Select	ENSP00000498939.1:p.Asn462Ile
ENST00000651783.1:c.926A>T	ENSP00000498924.1:p.Asn309Ile
ENST00000652018.1:c.1238A>T	ENSP00000498733.1:p.Asn413Ile
ENST00000336411.6:c.1385A>T	ENSP00000337915.2:p.Asn462Ile
ENST00000354593.6:c.935A>T	ENSP00000346607.2:p.Asn312Ile
NM_001202855.2:c.1382A>T	NP_001189784.1:p.Asn461Ile
NM_017460.5:c.1385A>T	NP_059488.2:p.Asn462Ile
XM_011515841.1:c.1478A>T	XP_011514143.1:p.Asn493Ile
XM_011515842.1:c.1475A>T	XP_011514144.1:p.Asn492Ile
NM_017460.6:c.1385A>T MANE Select	NP_059488.2:p.Asn462Ile
NM_001202855.3:c.1382A>T	NP_001189784.1:p.Asn461Ile