Canonical Allele Identifier: CA368367492

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99760817-A-C
• MyVariant Identifiers: chr7:g.99358440A>C (hg19) ; chr7:g.99760817A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760817A>C , CM000669.2:g.99760817A>C	GRCh38
NC_000007.13:g.99358440A>C , CM000669.1:g.99358440A>C	GRCh37
NC_000007.12:g.99196376A>C	NCBI36
NG_008421.1:g.28369T>G

Transcript Alleles

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