Canonical Allele Identifier: CA368367502

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358441C>A (hg19) ; chr7:g.99760818C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760818C>A , CM000669.2:g.99760818C>A	GRCh38
NC_000007.13:g.99358441C>A , CM000669.1:g.99358441C>A	GRCh37
NC_000007.12:g.99196377C>A	NCBI36
NG_008421.1:g.28368G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1509+1G>T	ENSP00000337915.3:n.1509+1G>T
ENST00000651162.1:n.851+1G>T
ENST00000651514.1:c.1416+1G>T MANE Select	ENSP00000498939.1:n.1416+1G>T
ENST00000651783.1:c.957+1G>T	ENSP00000498924.1:n.957+1G>T
ENST00000652018.1:c.1269+1G>T	ENSP00000498733.1:n.1269+1G>T
ENST00000336411.6:c.1416+1G>T	ENSP00000337915.2:n.1416+1G>T
ENST00000354593.6:c.966+1G>T	ENSP00000346607.2:n.966+1G>T
NM_001202855.2:c.1413+1G>T	NP_001189784.1:n.1413+1G>T
NM_017460.5:c.1416+1G>T	NP_059488.2:n.1416+1G>T
XM_011515841.1:c.1509+1G>T	XP_011514143.1:n.1509+1G>T
XM_011515842.1:c.1506+1G>T	XP_011514144.1:n.1506+1G>T
NM_017460.6:c.1416+1G>T MANE Select	NP_059488.2:n.1416+1G>T
NM_001202855.3:c.1413+1G>T	NP_001189784.1:n.1413+1G>T