Canonical Allele Identifier: CA456690887

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99770161-T-C
• MyVariant Identifiers: chr7:g.99367784T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770161T>C , CM000669.2:g.99770161T>C	GRCh38
NC_000007.13:g.99367784T>C , CM000669.1:g.99367784T>C	GRCh37
NC_000007.12:g.99205720T>C	NCBI36
NG_008421.1:g.19025A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.393A>G	ENSP00000337915.3:p.Ser131=
ENST00000651514.1:c.393A>G MANE Select	ENSP00000498939.1:p.Ser131=
ENST00000651783.1:c.58-1654A>G	ENSP00000498924.1:n.58-1654A>G
ENST00000652018.1:c.246A>G	ENSP00000498733.1:p.Ser82=
ENST00000336411.6:c.393A>G	ENSP00000337915.2:p.Ser131=
ENST00000354593.6:c.72-1659A>G	ENSP00000346607.2:n.72-1659A>G
ENST00000415003.1:c.432A>G	ENSP00000397208.1:p.Ser144=
ENST00000480043.1:n.290A>G
NM_001202855.2:c.393A>G	NP_001189784.1:p.Ser131=
NM_017460.5:c.393A>G	NP_059488.2:p.Ser131=
XM_011515841.1:c.393A>G	XP_011514143.1:p.Ser131=
XM_011515842.1:c.393A>G	XP_011514144.1:p.Ser131=
NM_017460.6:c.393A>G MANE Select	NP_059488.2:p.Ser131=
NM_001202855.3:c.393A>G	NP_001189784.1:p.Ser131=