Canonical Allele Identifier: CA368368658

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358551C>A (hg19) ; chr7:g.99760928C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760928C>A , CM000669.2:g.99760928C>A	GRCh38
NC_000007.13:g.99358551C>A , CM000669.1:g.99358551C>A	GRCh37
NC_000007.12:g.99196487C>A	NCBI36
NG_008421.1:g.28258G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1400G>T	ENSP00000337915.3:p.Gly467Val
ENST00000651162.1:n.742G>T
ENST00000651514.1:c.1307G>T MANE Select	ENSP00000498939.1:p.Gly436Val
ENST00000651783.1:c.848G>T	ENSP00000498924.1:p.Gly283Val
ENST00000652018.1:c.1160G>T	ENSP00000498733.1:p.Gly387Val
ENST00000336411.6:c.1307G>T	ENSP00000337915.2:p.Gly436Val
ENST00000354593.6:c.857G>T	ENSP00000346607.2:p.Gly286Val
NM_001202855.2:c.1304G>T	NP_001189784.1:p.Gly435Val
NM_017460.5:c.1307G>T	NP_059488.2:p.Gly436Val
XM_011515841.1:c.1400G>T	XP_011514143.1:p.Gly467Val
XM_011515842.1:c.1397G>T	XP_011514144.1:p.Gly466Val
NM_017460.6:c.1307G>T MANE Select	NP_059488.2:p.Gly436Val
NM_001202855.3:c.1304G>T	NP_001189784.1:p.Gly435Val