Canonical Allele Identifier: CA368372791

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99367403A>C (hg19) ; chr7:g.99769780A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769780A>C , CM000669.2:g.99769780A>C	GRCh38
NC_000007.13:g.99367403A>C , CM000669.1:g.99367403A>C	GRCh37
NC_000007.12:g.99205339A>C	NCBI36
NG_008421.1:g.19406T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.509T>G	ENSP00000337915.3:p.Val170Gly
ENST00000651514.1:c.509T>G MANE Select	ENSP00000498939.1:p.Val170Gly
ENST00000651783.1:c.58-1273T>G	ENSP00000498924.1:n.58-1273T>G
ENST00000652018.1:c.362T>G	ENSP00000498733.1:p.Val121Gly
ENST00000336411.6:c.509T>G	ENSP00000337915.2:p.Val170Gly
ENST00000354593.6:c.72-1278T>G	ENSP00000346607.2:n.72-1278T>G
ENST00000480043.1:n.406T>G
NM_001202855.2:c.509T>G	NP_001189784.1:p.Val170Gly
NM_017460.5:c.509T>G	NP_059488.2:p.Val170Gly
XM_011515841.1:c.509T>G	XP_011514143.1:p.Val170Gly
XM_011515842.1:c.509T>G	XP_011514144.1:p.Val170Gly
NM_017460.6:c.509T>G MANE Select	NP_059488.2:p.Val170Gly
NM_001202855.3:c.509T>G	NP_001189784.1:p.Val170Gly