Canonical Allele Identifier: CA1729176776

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760924A= , CM000669.2:g.99760924A=	GRCh38
NC_000007.13:g.99358547A= , CM000669.1:g.99358547A=	GRCh37
NC_000007.12:g.99196483A=	NCBI36
NG_008421.1:g.28262T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1404T=	ENSP00000337915.3:p.Ser468=
ENST00000651162.1:n.746T=
ENST00000651514.1:c.1311T= MANE Select	ENSP00000498939.1:p.Ser437=
ENST00000651783.1:c.852T=	ENSP00000498924.1:p.Ser284=
ENST00000652018.1:c.1164T=	ENSP00000498733.1:p.Ser388=
ENST00000336411.6:c.1311T=	ENSP00000337915.2:p.Ser437=
ENST00000354593.6:c.861T=	ENSP00000346607.2:p.Ser287=
NM_001202855.2:c.1308T=	NP_001189784.1:p.Ser436=
NM_017460.5:c.1311T=	NP_059488.2:p.Ser437=
XM_011515841.1:c.1404T=	XP_011514143.1:p.Ser468=
XM_011515842.1:c.1401T=	XP_011514144.1:p.Ser467=
NM_017460.6:c.1311T= MANE Select	NP_059488.2:p.Ser437=
NM_001202855.3:c.1308T=	NP_001189784.1:p.Ser436=