Canonical Allele Identifier: CA368370170

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99364764T>G (hg19) ; chr7:g.99767141T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767141T>G , CM000669.2:g.99767141T>G	GRCh38
NC_000007.13:g.99364764T>G , CM000669.1:g.99364764T>G	GRCh37
NC_000007.12:g.99202700T>G	NCBI36
NG_008421.1:g.22045A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.788A>C	ENSP00000337915.3:p.Asp263Ala
ENST00000651162.1:n.223A>C
ENST00000651514.1:c.788A>C MANE Select	ENSP00000498939.1:p.Asp263Ala
ENST00000651783.1:c.329A>C	ENSP00000498924.1:p.Asp110Ala
ENST00000652018.1:c.641A>C	ENSP00000498733.1:p.Asp214Ala
ENST00000336411.6:c.788A>C	ENSP00000337915.2:p.Asp263Ala
ENST00000354593.6:c.338A>C	ENSP00000346607.2:p.Asp113Ala
NM_001202855.2:c.785A>C	NP_001189784.1:p.Asp262Ala
NM_017460.5:c.788A>C	NP_059488.2:p.Asp263Ala
XM_011515841.1:c.788A>C	XP_011514143.1:p.Asp263Ala
XM_011515842.1:c.785A>C	XP_011514144.1:p.Asp262Ala
NM_017460.6:c.788A>C MANE Select	NP_059488.2:p.Asp263Ala
NM_001202855.3:c.785A>C	NP_001189784.1:p.Asp262Ala