Canonical Allele Identifier: CA368368724

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358582T>G (hg19) ; chr7:g.99760959T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760959T>G , CM000669.2:g.99760959T>G	GRCh38
NC_000007.13:g.99358582T>G , CM000669.1:g.99358582T>G	GRCh37
NC_000007.12:g.99196518T>G	NCBI36
NG_008421.1:g.28227A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1369A>C	ENSP00000337915.3:p.Asn457His
ENST00000651162.1:n.711A>C
ENST00000651514.1:c.1276A>C MANE Select	ENSP00000498939.1:p.Asn426His
ENST00000651783.1:c.817A>C	ENSP00000498924.1:p.Asn273His
ENST00000652018.1:c.1129A>C	ENSP00000498733.1:p.Asn377His
ENST00000336411.6:c.1276A>C	ENSP00000337915.2:p.Asn426His
ENST00000354593.6:c.826A>C	ENSP00000346607.2:p.Asn276His
NM_001202855.2:c.1273A>C	NP_001189784.1:p.Asn425His
NM_017460.5:c.1276A>C	NP_059488.2:p.Asn426His
XM_011515841.1:c.1369A>C	XP_011514143.1:p.Asn457His
XM_011515842.1:c.1366A>C	XP_011514144.1:p.Asn456His
NM_017460.6:c.1276A>C MANE Select	NP_059488.2:p.Asn426His
NM_001202855.3:c.1273A>C	NP_001189784.1:p.Asn425His