Canonical Allele Identifier: CA1729180919

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768436G= , CM000669.2:g.99768436G=	GRCh38
NC_000007.13:g.99366059G= , CM000669.1:g.99366059G=	GRCh37
NC_000007.12:g.99203995G=	NCBI36
NG_008421.1:g.20750C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.588C=	ENSP00000337915.3:p.Leu196=
ENST00000651514.1:c.588C= MANE Select	ENSP00000498939.1:p.Leu196=
ENST00000651783.1:c.129C=	ENSP00000498924.1:p.Leu43=
ENST00000652018.1:c.441C=	ENSP00000498733.1:p.Leu147=
ENST00000336411.6:c.588C=	ENSP00000337915.2:p.Leu196=
ENST00000354593.6:c.138C=	ENSP00000346607.2:p.Leu46=
NM_001202855.2:c.588C=	NP_001189784.1:p.Leu196=
NM_017460.5:c.588C=	NP_059488.2:p.Leu196=
XM_011515841.1:c.588C=	XP_011514143.1:p.Leu196=
XM_011515842.1:c.588C=	XP_011514144.1:p.Leu196=
NM_017460.6:c.588C= MANE Select	NP_059488.2:p.Leu196=
NM_001202855.3:c.588C=	NP_001189784.1:p.Leu196=