Canonical Allele Identifier: CA1729180902

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768430A= , CM000669.2:g.99768430A=	GRCh38
NC_000007.13:g.99366053A= , CM000669.1:g.99366053A=	GRCh37
NC_000007.12:g.99203989A=	NCBI36
NG_008421.1:g.20756T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.594T=	ENSP00000337915.3:p.Asn198=
ENST00000651514.1:c.594T= MANE Select	ENSP00000498939.1:p.Asn198=
ENST00000651783.1:c.135T=	ENSP00000498924.1:p.Asn45=
ENST00000652018.1:c.447T=	ENSP00000498733.1:p.Asn149=
ENST00000336411.6:c.594T=	ENSP00000337915.2:p.Asn198=
ENST00000354593.6:c.144T=	ENSP00000346607.2:p.Asn48=
NM_001202855.2:c.594T=	NP_001189784.1:p.Asn198=
NM_017460.5:c.594T=	NP_059488.2:p.Asn198=
XM_011515841.1:c.594T=	XP_011514143.1:p.Asn198=
XM_011515842.1:c.594T=	XP_011514144.1:p.Asn198=
NM_017460.6:c.594T= MANE Select	NP_059488.2:p.Asn198=
NM_001202855.3:c.594T=	NP_001189784.1:p.Asn198=