Canonical Allele Identifier: CA456689868

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99767223-A-G
• MyVariant Identifiers: chr7:g.99364846A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767223A>G , CM000669.2:g.99767223A>G	GRCh38
NC_000007.13:g.99364846A>G , CM000669.1:g.99364846A>G	GRCh37
NC_000007.12:g.99202782A>G	NCBI36
NG_008421.1:g.21963T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.706T>C	ENSP00000337915.3:p.Leu236=
ENST00000651162.1:n.141T>C
ENST00000651514.1:c.706T>C MANE Select	ENSP00000498939.1:p.Leu236=
ENST00000651783.1:c.247T>C	ENSP00000498924.1:p.Leu83=
ENST00000652018.1:c.559T>C	ENSP00000498733.1:p.Leu187=
ENST00000336411.6:c.706T>C	ENSP00000337915.2:p.Leu236=
ENST00000354593.6:c.256T>C	ENSP00000346607.2:p.Leu86=
NM_001202855.2:c.703T>C	NP_001189784.1:p.Leu235=
NM_017460.5:c.706T>C	NP_059488.2:p.Leu236=
XM_011515841.1:c.706T>C	XP_011514143.1:p.Leu236=
XM_011515842.1:c.703T>C	XP_011514144.1:p.Leu235=
NM_017460.6:c.706T>C MANE Select	NP_059488.2:p.Leu236=
NM_001202855.3:c.703T>C	NP_001189784.1:p.Leu235=