Canonical Allele Identifier: CA1729176757

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760880A= , CM000669.2:g.99760880A=	GRCh38
NC_000007.13:g.99358503A= , CM000669.1:g.99358503A=	GRCh37
NC_000007.12:g.99196439A=	NCBI36
NG_008421.1:g.28306T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1448T=	ENSP00000337915.3:p.Met483=
ENST00000651162.1:n.790T=
ENST00000651514.1:c.1355T= MANE Select	ENSP00000498939.1:p.Met452=
ENST00000651783.1:c.896T=	ENSP00000498924.1:p.Met299=
ENST00000652018.1:c.1208T=	ENSP00000498733.1:p.Met403=
ENST00000336411.6:c.1355T=	ENSP00000337915.2:p.Met452=
ENST00000354593.6:c.905T=	ENSP00000346607.2:p.Met302=
NM_001202855.2:c.1352T=	NP_001189784.1:p.Met451=
NM_017460.5:c.1355T=	NP_059488.2:p.Met452=
XM_011515841.1:c.1448T=	XP_011514143.1:p.Met483=
XM_011515842.1:c.1445T=	XP_011514144.1:p.Met482=
NM_017460.6:c.1355T= MANE Select	NP_059488.2:p.Met452=
NM_001202855.3:c.1352T=	NP_001189784.1:p.Met451=