Canonical Allele Identifier: CA1104975890

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815309792
• gnomAD v3: 7-99760994-T-A
• gnomAD v4: 7-99760994-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760994T>A , CM000669.2:g.99760994T>A	GRCh38
NC_000007.13:g.99358617T>A , CM000669.1:g.99358617T>A	GRCh37
NC_000007.12:g.99196553T>A	NCBI36
NG_008421.1:g.28192A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1347-13A>T	ENSP00000337915.3:n.1347-13A>T
ENST00000651162.1:n.689-13A>T
ENST00000651514.1:c.1254-13A>T MANE Select	ENSP00000498939.1:n.1254-13A>T
ENST00000651783.1:c.795-13A>T	ENSP00000498924.1:n.795-13A>T
ENST00000652018.1:c.1107-13A>T	ENSP00000498733.1:n.1107-13A>T
ENST00000336411.6:c.1254-13A>T	ENSP00000337915.2:n.1254-13A>T
ENST00000354593.6:c.804-13A>T	ENSP00000346607.2:n.804-13A>T
NM_001202855.2:c.1251-13A>T	NP_001189784.1:n.1251-13A>T
NM_017460.5:c.1254-13A>T	NP_059488.2:n.1254-13A>T
XM_011515841.1:c.1347-13A>T	XP_011514143.1:n.1347-13A>T
XM_011515842.1:c.1344-13A>T	XP_011514144.1:n.1344-13A>T
NM_017460.6:c.1254-13A>T MANE Select	NP_059488.2:n.1254-13A>T
NM_001202855.3:c.1251-13A>T	NP_001189784.1:n.1251-13A>T