Canonical Allele Identifier: CA1729182476

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770139T= , CM000669.2:g.99770139T=	GRCh38
NC_000007.13:g.99367762T= , CM000669.1:g.99367762T=	GRCh37
NC_000007.12:g.99205698T=	NCBI36
NG_008421.1:g.19047A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.415A=	ENSP00000337915.3:p.Ser139=
ENST00000651514.1:c.415A= MANE Select	ENSP00000498939.1:p.Ser139=
ENST00000651783.1:c.58-1632A=	ENSP00000498924.1:n.58-1632A=
ENST00000652018.1:c.268A=	ENSP00000498733.1:p.Ser90=
ENST00000336411.6:c.415A=	ENSP00000337915.2:p.Ser139=
ENST00000354593.6:c.72-1637A=	ENSP00000346607.2:n.72-1637A=
ENST00000415003.1:c.454A=	ENSP00000397208.1:p.Ser152=
ENST00000480043.1:n.312A=
NM_001202855.2:c.415A=	NP_001189784.1:p.Ser139=
NM_017460.5:c.415A=	NP_059488.2:p.Ser139=
XM_011515841.1:c.415A=	XP_011514143.1:p.Ser139=
XM_011515842.1:c.415A=	XP_011514144.1:p.Ser139=
NM_017460.6:c.415A= MANE Select	NP_059488.2:p.Ser139=
NM_001202855.3:c.415A=	NP_001189784.1:p.Ser139=