Canonical Allele Identifier: CA368370351

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99364844T>A (hg19) ; chr7:g.99767221T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767221T>A , CM000669.2:g.99767221T>A	GRCh38
NC_000007.13:g.99364844T>A , CM000669.1:g.99364844T>A	GRCh37
NC_000007.12:g.99202780T>A	NCBI36
NG_008421.1:g.21965A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.708A>T	ENSP00000337915.3:p.Leu236Phe
ENST00000651162.1:n.143A>T
ENST00000651514.1:c.708A>T MANE Select	ENSP00000498939.1:p.Leu236Phe
ENST00000651783.1:c.249A>T	ENSP00000498924.1:p.Leu83Phe
ENST00000652018.1:c.561A>T	ENSP00000498733.1:p.Leu187Phe
ENST00000336411.6:c.708A>T	ENSP00000337915.2:p.Leu236Phe
ENST00000354593.6:c.258A>T	ENSP00000346607.2:p.Leu86Phe
NM_001202855.2:c.705A>T	NP_001189784.1:p.Leu235Phe
NM_017460.5:c.708A>T	NP_059488.2:p.Leu236Phe
XM_011515841.1:c.708A>T	XP_011514143.1:p.Leu236Phe
XM_011515842.1:c.705A>T	XP_011514144.1:p.Leu235Phe
NM_017460.6:c.708A>T MANE Select	NP_059488.2:p.Leu236Phe
NM_001202855.3:c.705A>T	NP_001189784.1:p.Leu235Phe