Canonical Allele Identifier: CA1729176780

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760935G= , CM000669.2:g.99760935G=	GRCh38
NC_000007.13:g.99358558G= , CM000669.1:g.99358558G=	GRCh37
NC_000007.12:g.99196494G=	NCBI36
NG_008421.1:g.28251C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1393C=	ENSP00000337915.3:p.Pro465=
ENST00000651162.1:n.735C=
ENST00000651514.1:c.1300C= MANE Select	ENSP00000498939.1:p.Pro434=
ENST00000651783.1:c.841C=	ENSP00000498924.1:p.Pro281=
ENST00000652018.1:c.1153C=	ENSP00000498733.1:p.Pro385=
ENST00000336411.6:c.1300C=	ENSP00000337915.2:p.Pro434=
ENST00000354593.6:c.850C=	ENSP00000346607.2:p.Pro284=
NM_001202855.2:c.1297C=	NP_001189784.1:p.Pro433=
NM_017460.5:c.1300C=	NP_059488.2:p.Pro434=
XM_011515841.1:c.1393C=	XP_011514143.1:p.Pro465=
XM_011515842.1:c.1390C=	XP_011514144.1:p.Pro464=
NM_017460.6:c.1300C= MANE Select	NP_059488.2:p.Pro434=
NM_001202855.3:c.1297C=	NP_001189784.1:p.Pro433=