Canonical Allele Identifier: CA456686426

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358454A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760831A>G , CM000669.2:g.99760831A>G	GRCh38
NC_000007.13:g.99358454A>G , CM000669.1:g.99358454A>G	GRCh37
NC_000007.12:g.99196390A>G	NCBI36
NG_008421.1:g.28355T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1497T>C	ENSP00000337915.3:p.Cys499=
ENST00000651162.1:n.839T>C
ENST00000651514.1:c.1404T>C MANE Select	ENSP00000498939.1:p.Cys468=
ENST00000651783.1:c.945T>C	ENSP00000498924.1:p.Cys315=
ENST00000652018.1:c.1257T>C	ENSP00000498733.1:p.Cys419=
ENST00000336411.6:c.1404T>C	ENSP00000337915.2:p.Cys468=
ENST00000354593.6:c.954T>C	ENSP00000346607.2:p.Cys318=
NM_001202855.2:c.1401T>C	NP_001189784.1:p.Cys467=
NM_017460.5:c.1404T>C	NP_059488.2:p.Cys468=
XM_011515841.1:c.1497T>C	XP_011514143.1:p.Cys499=
XM_011515842.1:c.1494T>C	XP_011514144.1:p.Cys498=
NM_017460.6:c.1404T>C MANE Select	NP_059488.2:p.Cys468=
NM_001202855.3:c.1401T>C	NP_001189784.1:p.Cys467=