Canonical Allele Identifier: CA368373398

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99367774G>T (hg19) ; chr7:g.99770151G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770151G>T , CM000669.2:g.99770151G>T	GRCh38
NC_000007.13:g.99367774G>T , CM000669.1:g.99367774G>T	GRCh37
NC_000007.12:g.99205710G>T	NCBI36
NG_008421.1:g.19035C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.403C>A	ENSP00000337915.3:p.Pro135Thr
ENST00000651514.1:c.403C>A MANE Select	ENSP00000498939.1:p.Pro135Thr
ENST00000651783.1:c.58-1644C>A	ENSP00000498924.1:n.58-1644C>A
ENST00000652018.1:c.256C>A	ENSP00000498733.1:p.Pro86Thr
ENST00000336411.6:c.403C>A	ENSP00000337915.2:p.Pro135Thr
ENST00000354593.6:c.72-1649C>A	ENSP00000346607.2:n.72-1649C>A
ENST00000415003.1:c.442C>A	ENSP00000397208.1:p.Pro148Thr
ENST00000480043.1:n.300C>A
NM_001202855.2:c.403C>A	NP_001189784.1:p.Pro135Thr
NM_017460.5:c.403C>A	NP_059488.2:p.Pro135Thr
XM_011515841.1:c.403C>A	XP_011514143.1:p.Pro135Thr
XM_011515842.1:c.403C>A	XP_011514144.1:p.Pro135Thr
NM_017460.6:c.403C>A MANE Select	NP_059488.2:p.Pro135Thr
NM_001202855.3:c.403C>A	NP_001189784.1:p.Pro135Thr