Canonical Allele Identifier: CA368368552

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358504T>G (hg19) ; chr7:g.99760881T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760881T>G , CM000669.2:g.99760881T>G	GRCh38
NC_000007.13:g.99358504T>G , CM000669.1:g.99358504T>G	GRCh37
NC_000007.12:g.99196440T>G	NCBI36
NG_008421.1:g.28305A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1447A>C	ENSP00000337915.3:p.Met483Leu
ENST00000651162.1:n.789A>C
ENST00000651514.1:c.1354A>C MANE Select	ENSP00000498939.1:p.Met452Leu
ENST00000651783.1:c.895A>C	ENSP00000498924.1:p.Met299Leu
ENST00000652018.1:c.1207A>C	ENSP00000498733.1:p.Met403Leu
ENST00000336411.6:c.1354A>C	ENSP00000337915.2:p.Met452Leu
ENST00000354593.6:c.904A>C	ENSP00000346607.2:p.Met302Leu
NM_001202855.2:c.1351A>C	NP_001189784.1:p.Met451Leu
NM_017460.5:c.1354A>C	NP_059488.2:p.Met452Leu
XM_011515841.1:c.1447A>C	XP_011514143.1:p.Met483Leu
XM_011515842.1:c.1444A>C	XP_011514144.1:p.Met482Leu
NM_017460.6:c.1354A>C MANE Select	NP_059488.2:p.Met452Leu
NM_001202855.3:c.1351A>C	NP_001189784.1:p.Met451Leu