Canonical Allele Identifier: CA456686658

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358577T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760954T>G , CM000669.2:g.99760954T>G	GRCh38
NC_000007.13:g.99358577T>G , CM000669.1:g.99358577T>G	GRCh37
NC_000007.12:g.99196513T>G	NCBI36
NG_008421.1:g.28232A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1374A>C	ENSP00000337915.3:p.Ile458=
ENST00000651162.1:n.716A>C
ENST00000651514.1:c.1281A>C MANE Select	ENSP00000498939.1:p.Ile427=
ENST00000651783.1:c.822A>C	ENSP00000498924.1:p.Ile274=
ENST00000652018.1:c.1134A>C	ENSP00000498733.1:p.Ile378=
ENST00000336411.6:c.1281A>C	ENSP00000337915.2:p.Ile427=
ENST00000354593.6:c.831A>C	ENSP00000346607.2:p.Ile277=
NM_001202855.2:c.1278A>C	NP_001189784.1:p.Ile426=
NM_017460.5:c.1281A>C	NP_059488.2:p.Ile427=
XM_011515841.1:c.1374A>C	XP_011514143.1:p.Ile458=
XM_011515842.1:c.1371A>C	XP_011514144.1:p.Ile457=
NM_017460.6:c.1281A>C MANE Select	NP_059488.2:p.Ile427=
NM_001202855.3:c.1278A>C	NP_001189784.1:p.Ile426=