Canonical Allele Identifier: CA1729176801

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760975G= , CM000669.2:g.99760975G=	GRCh38
NC_000007.13:g.99358598G= , CM000669.1:g.99358598G=	GRCh37
NC_000007.12:g.99196534G=	NCBI36
NG_008421.1:g.28211C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1353C=	ENSP00000337915.3:p.Ser451=
ENST00000651162.1:n.695C=
ENST00000651514.1:c.1260C= MANE Select	ENSP00000498939.1:p.Ser420=
ENST00000651783.1:c.801C=	ENSP00000498924.1:p.Ser267=
ENST00000652018.1:c.1113C=	ENSP00000498733.1:p.Ser371=
ENST00000336411.6:c.1260C=	ENSP00000337915.2:p.Ser420=
ENST00000354593.6:c.810C=	ENSP00000346607.2:p.Ser270=
NM_001202855.2:c.1257C=	NP_001189784.1:p.Ser419=
NM_017460.5:c.1260C=	NP_059488.2:p.Ser420=
XM_011515841.1:c.1353C=	XP_011514143.1:p.Ser451=
XM_011515842.1:c.1350C=	XP_011514144.1:p.Ser450=
NM_017460.6:c.1260C= MANE Select	NP_059488.2:p.Ser420=
NM_001202855.3:c.1257C=	NP_001189784.1:p.Ser419=