Canonical Allele Identifier: CA368367605

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358465A>G (hg19) ; chr7:g.99760842A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760842A>G , CM000669.2:g.99760842A>G	GRCh38
NC_000007.13:g.99358465A>G , CM000669.1:g.99358465A>G	GRCh37
NC_000007.12:g.99196401A>G	NCBI36
NG_008421.1:g.28344T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1486T>C	ENSP00000337915.3:p.Phe496Leu
ENST00000651162.1:n.828T>C
ENST00000651514.1:c.1393T>C MANE Select	ENSP00000498939.1:p.Phe465Leu
ENST00000651783.1:c.934T>C	ENSP00000498924.1:p.Phe312Leu
ENST00000652018.1:c.1246T>C	ENSP00000498733.1:p.Phe416Leu
ENST00000336411.6:c.1393T>C	ENSP00000337915.2:p.Phe465Leu
ENST00000354593.6:c.943T>C	ENSP00000346607.2:p.Phe315Leu
NM_001202855.2:c.1390T>C	NP_001189784.1:p.Phe464Leu
NM_017460.5:c.1393T>C	NP_059488.2:p.Phe465Leu
XM_011515841.1:c.1486T>C	XP_011514143.1:p.Phe496Leu
XM_011515842.1:c.1483T>C	XP_011514144.1:p.Phe495Leu
NM_017460.6:c.1393T>C MANE Select	NP_059488.2:p.Phe465Leu
NM_001202855.3:c.1390T>C	NP_001189784.1:p.Phe464Leu