Canonical Allele Identifier: CA163151148

Gene: CYP3A4

Linked Data

• dbSNP Id: rs758878714
• MyVariant Identifiers: chr7:g.99358559T>C (hg19) ; chr7:g.99760936T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760936T>C , CM000669.2:g.99760936T>C	GRCh38
NC_000007.13:g.99358559T>C , CM000669.1:g.99358559T>C	GRCh37
NC_000007.12:g.99196495T>C	NCBI36
NG_008421.1:g.28250A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1392A>G	ENSP00000337915.3:p.Thr464=
ENST00000651162.1:n.734A>G
ENST00000651514.1:c.1299A>G MANE Select	ENSP00000498939.1:p.Thr433=
ENST00000651783.1:c.840A>G	ENSP00000498924.1:p.Thr280=
ENST00000652018.1:c.1152A>G	ENSP00000498733.1:p.Thr384=
ENST00000336411.6:c.1299A>G	ENSP00000337915.2:p.Thr433=
ENST00000354593.6:c.849A>G	ENSP00000346607.2:p.Thr283=
NM_001202855.2:c.1296A>G	NP_001189784.1:p.Thr432=
NM_017460.5:c.1299A>G	NP_059488.2:p.Thr433=
XM_011515841.1:c.1392A>G	XP_011514143.1:p.Thr464=
XM_011515842.1:c.1389A>G	XP_011514144.1:p.Thr463=
NM_017460.6:c.1299A>G MANE Select	NP_059488.2:p.Thr433=
NM_001202855.3:c.1296A>G	NP_001189784.1:p.Thr432=