Canonical Allele Identifier: CA1729177336

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762177G= , CM000669.2:g.99762177G=	GRCh38
NC_000007.13:g.99359800G= , CM000669.1:g.99359800G=	GRCh37
NC_000007.12:g.99197736G=	NCBI36
NG_008421.1:g.27009C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1117C=	ENSP00000337915.3:p.Leu373=
ENST00000651162.1:n.552C=
ENST00000651514.1:c.1117C= MANE Select	ENSP00000498939.1:p.Leu373=
ENST00000651783.1:c.658C=	ENSP00000498924.1:p.Leu220=
ENST00000652018.1:c.970C=	ENSP00000498733.1:p.Leu324=
ENST00000336411.6:c.1117C=	ENSP00000337915.2:p.Leu373=
ENST00000354593.6:c.667C=	ENSP00000346607.2:p.Leu223=
NM_001202855.2:c.1114C=	NP_001189784.1:p.Leu372=
NM_017460.5:c.1117C=	NP_059488.2:p.Leu373=
XM_011515841.1:c.1117C=	XP_011514143.1:p.Leu373=
XM_011515842.1:c.1114C=	XP_011514144.1:p.Leu372=
NM_017460.6:c.1117C= MANE Select	NP_059488.2:p.Leu373=
NM_001202855.3:c.1114C=	NP_001189784.1:p.Leu372=