Canonical Allele Identifier: CA368367723

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358495C>T (hg19) ; chr7:g.99760872C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760872C>T , CM000669.2:g.99760872C>T	GRCh38
NC_000007.13:g.99358495C>T , CM000669.1:g.99358495C>T	GRCh37
NC_000007.12:g.99196431C>T	NCBI36
NG_008421.1:g.28314G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1456G>A	ENSP00000337915.3:p.Ala486Thr
ENST00000651162.1:n.798G>A
ENST00000651514.1:c.1363G>A MANE Select	ENSP00000498939.1:p.Ala455Thr
ENST00000651783.1:c.904G>A	ENSP00000498924.1:p.Ala302Thr
ENST00000652018.1:c.1216G>A	ENSP00000498733.1:p.Ala406Thr
ENST00000336411.6:c.1363G>A	ENSP00000337915.2:p.Ala455Thr
ENST00000354593.6:c.913G>A	ENSP00000346607.2:p.Ala305Thr
NM_001202855.2:c.1360G>A	NP_001189784.1:p.Ala454Thr
NM_017460.5:c.1363G>A	NP_059488.2:p.Ala455Thr
XM_011515841.1:c.1456G>A	XP_011514143.1:p.Ala486Thr
XM_011515842.1:c.1453G>A	XP_011514144.1:p.Ala485Thr
NM_017460.6:c.1363G>A MANE Select	NP_059488.2:p.Ala455Thr
NM_001202855.3:c.1360G>A	NP_001189784.1:p.Ala454Thr