Canonical Allele Identifier: CA1729176756

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760876T= , CM000669.2:g.99760876T=	GRCh38
NC_000007.13:g.99358499T= , CM000669.1:g.99358499T=	GRCh37
NC_000007.12:g.99196435T=	NCBI36
NG_008421.1:g.28310A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1452A=	ENSP00000337915.3:p.Lys484=
ENST00000651162.1:n.794A=
ENST00000651514.1:c.1359A= MANE Select	ENSP00000498939.1:p.Lys453=
ENST00000651783.1:c.900A=	ENSP00000498924.1:p.Lys300=
ENST00000652018.1:c.1212A=	ENSP00000498733.1:p.Lys404=
ENST00000336411.6:c.1359A=	ENSP00000337915.2:p.Lys453=
ENST00000354593.6:c.909A=	ENSP00000346607.2:p.Lys303=
NM_001202855.2:c.1356A=	NP_001189784.1:p.Lys452=
NM_017460.5:c.1359A=	NP_059488.2:p.Lys453=
XM_011515841.1:c.1452A=	XP_011514143.1:p.Lys484=
XM_011515842.1:c.1449A=	XP_011514144.1:p.Lys483=
NM_017460.6:c.1359A= MANE Select	NP_059488.2:p.Lys453=
NM_001202855.3:c.1356A=	NP_001189784.1:p.Lys452=