Canonical Allele Identifier: CA1729179909

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767115_99767118delinsTACC , CM000669.2:g.99767115_99767118delinsTACC	GRCh38
NC_000007.13:g.99364738_99364741delinsTACC , CM000669.1:g.99364738_99364741delinsTACC	GRCh37
NC_000007.12:g.99202674_99202677delinsTACC	NCBI36
NG_008421.1:g.22068_22071delinsGGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.798+13_798+16delinsGGTA	ENSP00000337915.3:n.798+13_798+16delinsGGTA
ENST00000651162.1:n.233+13_233+16delinsGGTA
ENST00000651514.1:c.798+13_798+16delinsGGTA MANE Select	ENSP00000498939.1:n.798+13_798+16delinsGGTA
ENST00000651783.1:c.339+13_339+16delinsGGTA	ENSP00000498924.1:n.339+13_339+16delinsGGTA
ENST00000652018.1:c.651+13_651+16delinsGGTA	ENSP00000498733.1:n.651+13_651+16delinsGGTA
ENST00000336411.6:c.798+13_798+16delinsGGTA	ENSP00000337915.2:n.798+13_798+16delinsGGTA
ENST00000354593.6:c.348+13_348+16delinsGGTA	ENSP00000346607.2:n.348+13_348+16delinsGGTA
NM_001202855.2:c.795+13_795+16delinsGGTA	NP_001189784.1:n.795+13_795+16delinsGGTA
NM_017460.5:c.798+13_798+16delinsGGTA	NP_059488.2:n.798+13_798+16delinsGGTA
XM_011515841.1:c.798+13_798+16delinsGGTA	XP_011514143.1:n.798+13_798+16delinsGGTA
XM_011515842.1:c.795+13_795+16delinsGGTA	XP_011514144.1:n.795+13_795+16delinsGGTA
NM_017460.6:c.798+13_798+16delinsGGTA MANE Select	NP_059488.2:n.798+13_798+16delinsGGTA
NM_001202855.3:c.795+13_795+16delinsGGTA	NP_001189784.1:n.795+13_795+16delinsGGTA