Canonical Allele Identifier: CA456686468

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99760869-G-A
• MyVariant Identifiers: chr7:g.99358492G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760869G>A , CM000669.2:g.99760869G>A	GRCh38
NC_000007.13:g.99358492G>A , CM000669.1:g.99358492G>A	GRCh37
NC_000007.12:g.99196428G>A	NCBI36
NG_008421.1:g.28317C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1459C>T	ENSP00000337915.3:p.Leu487=
ENST00000651162.1:n.801C>T
ENST00000651514.1:c.1366C>T MANE Select	ENSP00000498939.1:p.Leu456=
ENST00000651783.1:c.907C>T	ENSP00000498924.1:p.Leu303=
ENST00000652018.1:c.1219C>T	ENSP00000498733.1:p.Leu407=
ENST00000336411.6:c.1366C>T	ENSP00000337915.2:p.Leu456=
ENST00000354593.6:c.916C>T	ENSP00000346607.2:p.Leu306=
NM_001202855.2:c.1363C>T	NP_001189784.1:p.Leu455=
NM_017460.5:c.1366C>T	NP_059488.2:p.Leu456=
XM_011515841.1:c.1459C>T	XP_011514143.1:p.Leu487=
XM_011515842.1:c.1456C>T	XP_011514144.1:p.Leu486=
NM_017460.6:c.1366C>T MANE Select	NP_059488.2:p.Leu456=
NM_001202855.3:c.1363C>T	NP_001189784.1:p.Leu455=