Canonical Allele Identifier: CA368368688

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358565T>C (hg19) ; chr7:g.99760942T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760942T>C , CM000669.2:g.99760942T>C	GRCh38
NC_000007.13:g.99358565T>C , CM000669.1:g.99358565T>C	GRCh37
NC_000007.12:g.99196501T>C	NCBI36
NG_008421.1:g.28244A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1386A>G	ENSP00000337915.3:p.Ile462Met
ENST00000651162.1:n.728A>G
ENST00000651514.1:c.1293A>G MANE Select	ENSP00000498939.1:p.Ile431Met
ENST00000651783.1:c.834A>G	ENSP00000498924.1:p.Ile278Met
ENST00000652018.1:c.1146A>G	ENSP00000498733.1:p.Ile382Met
ENST00000336411.6:c.1293A>G	ENSP00000337915.2:p.Ile431Met
ENST00000354593.6:c.843A>G	ENSP00000346607.2:p.Ile281Met
NM_001202855.2:c.1290A>G	NP_001189784.1:p.Ile430Met
NM_017460.5:c.1293A>G	NP_059488.2:p.Ile431Met
XM_011515841.1:c.1386A>G	XP_011514143.1:p.Ile462Met
XM_011515842.1:c.1383A>G	XP_011514144.1:p.Ile461Met
NM_017460.6:c.1293A>G MANE Select	NP_059488.2:p.Ile431Met
NM_001202855.3:c.1290A>G	NP_001189784.1:p.Ile430Met