Canonical Allele Identifier: CA2683985401

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99760990-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760990A>G , CM000669.2:g.99760990A>G	GRCh38
NC_000007.13:g.99358613A>G , CM000669.1:g.99358613A>G	GRCh37
NC_000007.12:g.99196549A>G	NCBI36
NG_008421.1:g.28196T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1347-9T>C	ENSP00000337915.3:n.1347-9T>C
ENST00000651162.1:n.689-9T>C
ENST00000651514.1:c.1254-9T>C MANE Select	ENSP00000498939.1:n.1254-9T>C
ENST00000651783.1:c.795-9T>C	ENSP00000498924.1:n.795-9T>C
ENST00000652018.1:c.1107-9T>C	ENSP00000498733.1:n.1107-9T>C
ENST00000336411.6:c.1254-9T>C	ENSP00000337915.2:n.1254-9T>C
ENST00000354593.6:c.804-9T>C	ENSP00000346607.2:n.804-9T>C
NM_001202855.2:c.1251-9T>C	NP_001189784.1:n.1251-9T>C
NM_017460.5:c.1254-9T>C	NP_059488.2:n.1254-9T>C
XM_011515841.1:c.1347-9T>C	XP_011514143.1:n.1347-9T>C
XM_011515842.1:c.1344-9T>C	XP_011514144.1:n.1344-9T>C
NM_017460.6:c.1254-9T>C MANE Select	NP_059488.2:n.1254-9T>C
NM_001202855.3:c.1251-9T>C	NP_001189784.1:n.1251-9T>C