Canonical Allele Identifier: CA368368620

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358534A>G (hg19) ; chr7:g.99760911A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760911A>G , CM000669.2:g.99760911A>G	GRCh38
NC_000007.13:g.99358534A>G , CM000669.1:g.99358534A>G	GRCh37
NC_000007.12:g.99196470A>G	NCBI36
NG_008421.1:g.28275T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1417T>C	ENSP00000337915.3:p.Cys473Arg
ENST00000651162.1:n.759T>C
ENST00000651514.1:c.1324T>C MANE Select	ENSP00000498939.1:p.Cys442Arg
ENST00000651783.1:c.865T>C	ENSP00000498924.1:p.Cys289Arg
ENST00000652018.1:c.1177T>C	ENSP00000498733.1:p.Cys393Arg
ENST00000336411.6:c.1324T>C	ENSP00000337915.2:p.Cys442Arg
ENST00000354593.6:c.874T>C	ENSP00000346607.2:p.Cys292Arg
NM_001202855.2:c.1321T>C	NP_001189784.1:p.Cys441Arg
NM_017460.5:c.1324T>C	NP_059488.2:p.Cys442Arg
XM_011515841.1:c.1417T>C	XP_011514143.1:p.Cys473Arg
XM_011515842.1:c.1414T>C	XP_011514144.1:p.Cys472Arg
NM_017460.6:c.1324T>C MANE Select	NP_059488.2:p.Cys442Arg
NM_001202855.3:c.1321T>C	NP_001189784.1:p.Cys441Arg