Canonical Allele Identifier: CA1729176789

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760951A= , CM000669.2:g.99760951A=	GRCh38
NC_000007.13:g.99358574A= , CM000669.1:g.99358574A=	GRCh37
NC_000007.12:g.99196510A=	NCBI36
NG_008421.1:g.28235T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1377T=	ENSP00000337915.3:p.Asp459=
ENST00000651162.1:n.719T=
ENST00000651514.1:c.1284T= MANE Select	ENSP00000498939.1:p.Asp428=
ENST00000651783.1:c.825T=	ENSP00000498924.1:p.Asp275=
ENST00000652018.1:c.1137T=	ENSP00000498733.1:p.Asp379=
ENST00000336411.6:c.1284T=	ENSP00000337915.2:p.Asp428=
ENST00000354593.6:c.834T=	ENSP00000346607.2:p.Asp278=
NM_001202855.2:c.1281T=	NP_001189784.1:p.Asp427=
NM_017460.5:c.1284T=	NP_059488.2:p.Asp428=
XM_011515841.1:c.1377T=	XP_011514143.1:p.Asp459=
XM_011515842.1:c.1374T=	XP_011514144.1:p.Asp458=
NM_017460.6:c.1284T= MANE Select	NP_059488.2:p.Asp428=
NM_001202855.3:c.1281T=	NP_001189784.1:p.Asp427=