Canonical Allele Identifier: CA368368624

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358536T>A (hg19) ; chr7:g.99760913T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760913T>A , CM000669.2:g.99760913T>A	GRCh38
NC_000007.13:g.99358536T>A , CM000669.1:g.99358536T>A	GRCh37
NC_000007.12:g.99196472T>A	NCBI36
NG_008421.1:g.28273A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1415A>T	ENSP00000337915.3:p.Asn472Ile
ENST00000651162.1:n.757A>T
ENST00000651514.1:c.1322A>T MANE Select	ENSP00000498939.1:p.Asn441Ile
ENST00000651783.1:c.863A>T	ENSP00000498924.1:p.Asn288Ile
ENST00000652018.1:c.1175A>T	ENSP00000498733.1:p.Asn392Ile
ENST00000336411.6:c.1322A>T	ENSP00000337915.2:p.Asn441Ile
ENST00000354593.6:c.872A>T	ENSP00000346607.2:p.Asn291Ile
NM_001202855.2:c.1319A>T	NP_001189784.1:p.Asn440Ile
NM_017460.5:c.1322A>T	NP_059488.2:p.Asn441Ile
XM_011515841.1:c.1415A>T	XP_011514143.1:p.Asn472Ile
XM_011515842.1:c.1412A>T	XP_011514144.1:p.Asn471Ile
NM_017460.6:c.1322A>T MANE Select	NP_059488.2:p.Asn441Ile
NM_001202855.3:c.1319A>T	NP_001189784.1:p.Asn440Ile