Canonical Allele Identifier: CA368367663

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358479A>C (hg19) ; chr7:g.99760856A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760856A>C , CM000669.2:g.99760856A>C	GRCh38
NC_000007.13:g.99358479A>C , CM000669.1:g.99358479A>C	GRCh37
NC_000007.12:g.99196415A>C	NCBI36
NG_008421.1:g.28330T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1472T>G	ENSP00000337915.3:p.Leu491Arg
ENST00000651162.1:n.814T>G
ENST00000651514.1:c.1379T>G MANE Select	ENSP00000498939.1:p.Leu460Arg
ENST00000651783.1:c.920T>G	ENSP00000498924.1:p.Leu307Arg
ENST00000652018.1:c.1232T>G	ENSP00000498733.1:p.Leu411Arg
ENST00000336411.6:c.1379T>G	ENSP00000337915.2:p.Leu460Arg
ENST00000354593.6:c.929T>G	ENSP00000346607.2:p.Leu310Arg
NM_001202855.2:c.1376T>G	NP_001189784.1:p.Leu459Arg
NM_017460.5:c.1379T>G	NP_059488.2:p.Leu460Arg
XM_011515841.1:c.1472T>G	XP_011514143.1:p.Leu491Arg
XM_011515842.1:c.1469T>G	XP_011514144.1:p.Leu490Arg
NM_017460.6:c.1379T>G MANE Select	NP_059488.2:p.Leu460Arg
NM_001202855.3:c.1376T>G	NP_001189784.1:p.Leu459Arg