Canonical Allele Identifier: CA1729182521

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770162G= , CM000669.2:g.99770162G=	GRCh38
NC_000007.13:g.99367785G= , CM000669.1:g.99367785G=	GRCh37
NC_000007.12:g.99205721G=	NCBI36
NG_008421.1:g.19024C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.392C=	ENSP00000337915.3:p.Ser131=
ENST00000651514.1:c.392C= MANE Select	ENSP00000498939.1:p.Ser131=
ENST00000651783.1:c.58-1655C=	ENSP00000498924.1:n.58-1655C=
ENST00000652018.1:c.245C=	ENSP00000498733.1:p.Ser82=
ENST00000336411.6:c.392C=	ENSP00000337915.2:p.Ser131=
ENST00000354593.6:c.72-1660C=	ENSP00000346607.2:n.72-1660C=
ENST00000415003.1:c.431C=	ENSP00000397208.1:p.Ser144=
ENST00000480043.1:n.289C=
NM_001202855.2:c.392C=	NP_001189784.1:p.Ser131=
NM_017460.5:c.392C=	NP_059488.2:p.Ser131=
XM_011515841.1:c.392C=	XP_011514143.1:p.Ser131=
XM_011515842.1:c.392C=	XP_011514144.1:p.Ser131=
NM_017460.6:c.392C= MANE Select	NP_059488.2:p.Ser131=
NM_001202855.3:c.392C=	NP_001189784.1:p.Ser131=