Canonical Allele Identifier: CA456686450

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358475C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760852C>T , CM000669.2:g.99760852C>T	GRCh38
NC_000007.13:g.99358475C>T , CM000669.1:g.99358475C>T	GRCh37
NC_000007.12:g.99196411C>T	NCBI36
NG_008421.1:g.28334G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1476G>A	ENSP00000337915.3:p.Gln492=
ENST00000651162.1:n.818G>A
ENST00000651514.1:c.1383G>A MANE Select	ENSP00000498939.1:p.Gln461=
ENST00000651783.1:c.924G>A	ENSP00000498924.1:p.Gln308=
ENST00000652018.1:c.1236G>A	ENSP00000498733.1:p.Gln412=
ENST00000336411.6:c.1383G>A	ENSP00000337915.2:p.Gln461=
ENST00000354593.6:c.933G>A	ENSP00000346607.2:p.Gln311=
NM_001202855.2:c.1380G>A	NP_001189784.1:p.Gln460=
NM_017460.5:c.1383G>A	NP_059488.2:p.Gln461=
XM_011515841.1:c.1476G>A	XP_011514143.1:p.Gln492=
XM_011515842.1:c.1473G>A	XP_011514144.1:p.Gln491=
NM_017460.6:c.1383G>A MANE Select	NP_059488.2:p.Gln461=
NM_001202855.3:c.1380G>A	NP_001189784.1:p.Gln460=