Canonical Allele Identifier: CA2777129116

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760774A>C , CM000669.2:g.99760774A>C	GRCh38
NC_000007.13:g.99358397A>C , CM000669.1:g.99358397A>C	GRCh37
NC_000007.12:g.99196333A>C	NCBI36
NG_008421.1:g.28412T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1509+45T>G	ENSP00000337915.3:n.1509+45T>G
ENST00000651162.1:n.851+45T>G
ENST00000651514.1:c.1416+45T>G MANE Select	ENSP00000498939.1:n.1416+45T>G
ENST00000651783.1:c.957+45T>G	ENSP00000498924.1:n.957+45T>G
ENST00000652018.1:c.1269+45T>G	ENSP00000498733.1:n.1269+45T>G
ENST00000336411.6:c.1416+45T>G	ENSP00000337915.2:n.1416+45T>G
ENST00000354593.6:c.966+45T>G	ENSP00000346607.2:n.966+45T>G
NM_001202855.2:c.1413+45T>G	NP_001189784.1:n.1413+45T>G
NM_017460.5:c.1416+45T>G	NP_059488.2:n.1416+45T>G
XM_011515841.1:c.1509+45T>G	XP_011514143.1:n.1509+45T>G
XM_011515842.1:c.1506+45T>G	XP_011514144.1:n.1506+45T>G
NM_017460.6:c.1416+45T>G MANE Select	NP_059488.2:n.1416+45T>G
NM_001202855.3:c.1413+45T>G	NP_001189784.1:n.1413+45T>G