Canonical Allele Identifier: CA368369022

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99359739A>G (hg19) ; chr7:g.99762116A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762116A>G , CM000669.2:g.99762116A>G	GRCh38
NC_000007.13:g.99359739A>G , CM000669.1:g.99359739A>G	GRCh37
NC_000007.12:g.99197675A>G	NCBI36
NG_008421.1:g.27070T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1178T>C	ENSP00000337915.3:p.Val393Ala
ENST00000651162.1:n.613T>C
ENST00000651514.1:c.1178T>C MANE Select	ENSP00000498939.1:p.Val393Ala
ENST00000651783.1:c.719T>C	ENSP00000498924.1:p.Val240Ala
ENST00000652018.1:c.1031T>C	ENSP00000498733.1:p.Val344Ala
ENST00000336411.6:c.1178T>C	ENSP00000337915.2:p.Val393Ala
ENST00000354593.6:c.728T>C	ENSP00000346607.2:p.Val243Ala
NM_001202855.2:c.1175T>C	NP_001189784.1:p.Val392Ala
NM_017460.5:c.1178T>C	NP_059488.2:p.Val393Ala
XM_011515841.1:c.1178T>C	XP_011514143.1:p.Val393Ala
XM_011515842.1:c.1175T>C	XP_011514144.1:p.Val392Ala
NM_017460.6:c.1178T>C MANE Select	NP_059488.2:p.Val393Ala
NM_001202855.3:c.1175T>C	NP_001189784.1:p.Val392Ala