Canonical Allele Identifier: CA456687148

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99359705G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762082G>A , CM000669.2:g.99762082G>A	GRCh38
NC_000007.13:g.99359705G>A , CM000669.1:g.99359705G>A	GRCh37
NC_000007.12:g.99197641G>A	NCBI36
NG_008421.1:g.27104C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1212C>T	ENSP00000337915.3:p.Asp404=
ENST00000651162.1:n.647C>T
ENST00000651514.1:c.1212C>T MANE Select	ENSP00000498939.1:p.Asp404=
ENST00000651783.1:c.753C>T	ENSP00000498924.1:p.Asp251=
ENST00000652018.1:c.1065C>T	ENSP00000498733.1:p.Asp355=
ENST00000336411.6:c.1212C>T	ENSP00000337915.2:p.Asp404=
ENST00000354593.6:c.762C>T	ENSP00000346607.2:p.Asp254=
NM_001202855.2:c.1209C>T	NP_001189784.1:p.Asp403=
NM_017460.5:c.1212C>T	NP_059488.2:p.Asp404=
XM_011515841.1:c.1212C>T	XP_011514143.1:p.Asp404=
XM_011515842.1:c.1209C>T	XP_011514144.1:p.Asp403=
NM_017460.6:c.1212C>T MANE Select	NP_059488.2:p.Asp404=
NM_001202855.3:c.1209C>T	NP_001189784.1:p.Asp403=