Canonical Allele Identifier: CA1729177312

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762111T= , CM000669.2:g.99762111T=	GRCh38
NC_000007.13:g.99359734T= , CM000669.1:g.99359734T=	GRCh37
NC_000007.12:g.99197670T=	NCBI36
NG_008421.1:g.27075A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1183A=	ENSP00000337915.3:p.Met395=
ENST00000651162.1:n.618A=
ENST00000651514.1:c.1183A= MANE Select	ENSP00000498939.1:p.Met395=
ENST00000651783.1:c.724A=	ENSP00000498924.1:p.Met242=
ENST00000652018.1:c.1036A=	ENSP00000498733.1:p.Met346=
ENST00000336411.6:c.1183A=	ENSP00000337915.2:p.Met395=
ENST00000354593.6:c.733A=	ENSP00000346607.2:p.Met245=
NM_001202855.2:c.1180A=	NP_001189784.1:p.Met394=
NM_017460.5:c.1183A=	NP_059488.2:p.Met395=
XM_011515841.1:c.1183A=	XP_011514143.1:p.Met395=
XM_011515842.1:c.1180A=	XP_011514144.1:p.Met394=
NM_017460.6:c.1183A= MANE Select	NP_059488.2:p.Met395=
NM_001202855.3:c.1180A=	NP_001189784.1:p.Met394=