Canonical Allele Identifier: CA456686620
Gene: CYP3A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.99358544T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99760921T>A , CM000669.2:g.99760921T>A GRCh38
NC_000007.13:g.99358544T>A , CM000669.1:g.99358544T>A GRCh37
NC_000007.12:g.99196480T>A NCBI36
NG_008421.1:g.28265A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.1407A>T ENSP00000337915.3:p.Gly469=
ENST00000651162.1:n.749A>T
ENST00000651514.1:c.1314A>T MANE Select ENSP00000498939.1:p.Gly438=
ENST00000651783.1:c.855A>T ENSP00000498924.1:p.Gly285=
ENST00000652018.1:c.1167A>T ENSP00000498733.1:p.Gly389=
ENST00000336411.6:c.1314A>T ENSP00000337915.2:p.Gly438=
ENST00000354593.6:c.864A>T ENSP00000346607.2:p.Gly288=
NM_001202855.2:c.1311A>T NP_001189784.1:p.Gly437=
NM_017460.5:c.1314A>T NP_059488.2:p.Gly438=
XM_011515841.1:c.1407A>T XP_011514143.1:p.Gly469=
XM_011515842.1:c.1404A>T XP_011514144.1:p.Gly468=
NM_017460.6:c.1314A>T MANE Select NP_059488.2:p.Gly438=
NM_001202855.3:c.1311A>T NP_001189784.1:p.Gly437=