Canonical Allele Identifier: CA456690136

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99366026G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768403G>C , CM000669.2:g.99768403G>C	GRCh38
NC_000007.13:g.99366026G>C , CM000669.1:g.99366026G>C	GRCh37
NC_000007.12:g.99203962G>C	NCBI36
NG_008421.1:g.20783C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.621C>G	ENSP00000337915.3:p.Thr207=
ENST00000651514.1:c.621C>G MANE Select	ENSP00000498939.1:p.Thr207=
ENST00000651783.1:c.162C>G	ENSP00000498924.1:p.Thr54=
ENST00000652018.1:c.474C>G	ENSP00000498733.1:p.Thr158=
ENST00000336411.6:c.621C>G	ENSP00000337915.2:p.Thr207=
ENST00000354593.6:c.171C>G	ENSP00000346607.2:p.Thr57=
NM_001202855.2:c.621C>G	NP_001189784.1:p.Thr207=
NM_017460.5:c.621C>G	NP_059488.2:p.Thr207=
XM_011515841.1:c.621C>G	XP_011514143.1:p.Thr207=
XM_011515842.1:c.621C>G	XP_011514144.1:p.Thr207=
NM_017460.6:c.621C>G MANE Select	NP_059488.2:p.Thr207=
NM_001202855.3:c.621C>G	NP_001189784.1:p.Thr207=