Canonical Allele Identifier: CA368368635

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358540T>C (hg19) ; chr7:g.99760917T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760917T>C , CM000669.2:g.99760917T>C	GRCh38
NC_000007.13:g.99358540T>C , CM000669.1:g.99358540T>C	GRCh37
NC_000007.12:g.99196476T>C	NCBI36
NG_008421.1:g.28269A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1411A>G	ENSP00000337915.3:p.Arg471Gly
ENST00000651162.1:n.753A>G
ENST00000651514.1:c.1318A>G MANE Select	ENSP00000498939.1:p.Arg440Gly
ENST00000651783.1:c.859A>G	ENSP00000498924.1:p.Arg287Gly
ENST00000652018.1:c.1171A>G	ENSP00000498733.1:p.Arg391Gly
ENST00000336411.6:c.1318A>G	ENSP00000337915.2:p.Arg440Gly
ENST00000354593.6:c.868A>G	ENSP00000346607.2:p.Arg290Gly
NM_001202855.2:c.1315A>G	NP_001189784.1:p.Arg439Gly
NM_017460.5:c.1318A>G	NP_059488.2:p.Arg440Gly
XM_011515841.1:c.1411A>G	XP_011514143.1:p.Arg471Gly
XM_011515842.1:c.1408A>G	XP_011514144.1:p.Arg470Gly
NM_017460.6:c.1318A>G MANE Select	NP_059488.2:p.Arg440Gly
NM_001202855.3:c.1315A>G	NP_001189784.1:p.Arg439Gly