Canonical Allele Identifier: CA368370302

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99767199-C-A
• COSMIC: COSM1093884
• MyVariant Identifiers: chr7:g.99364822C>A (hg19) ; chr7:g.99767199C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767199C>A , CM000669.2:g.99767199C>A	GRCh38
NC_000007.13:g.99364822C>A , CM000669.1:g.99364822C>A	GRCh37
NC_000007.12:g.99202758C>A	NCBI36
NG_008421.1:g.21987G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.730G>T	ENSP00000337915.3:p.Glu244Ter
ENST00000651162.1:n.165G>T
ENST00000651514.1:c.730G>T MANE Select	ENSP00000498939.1:p.Glu244Ter
ENST00000651783.1:c.271G>T	ENSP00000498924.1:p.Glu91Ter
ENST00000652018.1:c.583G>T	ENSP00000498733.1:p.Glu195Ter
ENST00000336411.6:c.730G>T	ENSP00000337915.2:p.Glu244Ter
ENST00000354593.6:c.280G>T	ENSP00000346607.2:p.Glu94Ter
NM_001202855.2:c.727G>T	NP_001189784.1:p.Glu243Ter
NM_017460.5:c.730G>T	NP_059488.2:p.Glu244Ter
XM_011515841.1:c.730G>T	XP_011514143.1:p.Glu244Ter
XM_011515842.1:c.727G>T	XP_011514144.1:p.Glu243Ter
NM_017460.6:c.730G>T MANE Select	NP_059488.2:p.Glu244Ter
NM_001202855.3:c.727G>T	NP_001189784.1:p.Glu243Ter