Canonical Allele Identifier: CA368368659

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358552C>A (hg19) ; chr7:g.99760929C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760929C>A , CM000669.2:g.99760929C>A	GRCh38
NC_000007.13:g.99358552C>A , CM000669.1:g.99358552C>A	GRCh37
NC_000007.12:g.99196488C>A	NCBI36
NG_008421.1:g.28257G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1399G>T	ENSP00000337915.3:p.Gly467Ter
ENST00000651162.1:n.741G>T
ENST00000651514.1:c.1306G>T MANE Select	ENSP00000498939.1:p.Gly436Ter
ENST00000651783.1:c.847G>T	ENSP00000498924.1:p.Gly283Ter
ENST00000652018.1:c.1159G>T	ENSP00000498733.1:p.Gly387Ter
ENST00000336411.6:c.1306G>T	ENSP00000337915.2:p.Gly436Ter
ENST00000354593.6:c.856G>T	ENSP00000346607.2:p.Gly286Ter
NM_001202855.2:c.1303G>T	NP_001189784.1:p.Gly435Ter
NM_017460.5:c.1306G>T	NP_059488.2:p.Gly436Ter
XM_011515841.1:c.1399G>T	XP_011514143.1:p.Gly467Ter
XM_011515842.1:c.1396G>T	XP_011514144.1:p.Gly466Ter
NM_017460.6:c.1306G>T MANE Select	NP_059488.2:p.Gly436Ter
NM_001202855.3:c.1303G>T	NP_001189784.1:p.Gly435Ter