Canonical Allele Identifier: CA368373168

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99367477C>A (hg19) ; chr7:g.99769854C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769854C>A , CM000669.2:g.99769854C>A	GRCh38
NC_000007.13:g.99367477C>A , CM000669.1:g.99367477C>A	GRCh37
NC_000007.12:g.99205413C>A	NCBI36
NG_008421.1:g.19332G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.435G>T	ENSP00000337915.3:p.Met145Ile
ENST00000651514.1:c.435G>T MANE Select	ENSP00000498939.1:p.Met145Ile
ENST00000651783.1:c.58-1347G>T	ENSP00000498924.1:n.58-1347G>T
ENST00000652018.1:c.288G>T	ENSP00000498733.1:p.Met96Ile
ENST00000336411.6:c.435G>T	ENSP00000337915.2:p.Met145Ile
ENST00000354593.6:c.72-1352G>T	ENSP00000346607.2:n.72-1352G>T
ENST00000480043.1:n.332G>T
NM_001202855.2:c.435G>T	NP_001189784.1:p.Met145Ile
NM_017460.5:c.435G>T	NP_059488.2:p.Met145Ile
XM_011515841.1:c.435G>T	XP_011514143.1:p.Met145Ile
XM_011515842.1:c.435G>T	XP_011514144.1:p.Met145Ile
NM_017460.6:c.435G>T MANE Select	NP_059488.2:p.Met145Ile
NM_001202855.3:c.435G>T	NP_001189784.1:p.Met145Ile