Canonical Allele Identifier: CA2683986528

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99769991-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769991T>A , CM000669.2:g.99769991T>A	GRCh38
NC_000007.13:g.99367614T>A , CM000669.1:g.99367614T>A	GRCh37
NC_000007.12:g.99205550T>A	NCBI36
NG_008421.1:g.19195A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.432+131A>T	ENSP00000337915.3:n.432+131A>T
ENST00000651514.1:c.432+131A>T MANE Select	ENSP00000498939.1:n.432+131A>T
ENST00000651783.1:c.58-1484A>T	ENSP00000498924.1:n.58-1484A>T
ENST00000652018.1:c.285+131A>T	ENSP00000498733.1:n.285+131A>T
ENST00000336411.6:c.432+131A>T	ENSP00000337915.2:n.432+131A>T
ENST00000354593.6:c.72-1489A>T	ENSP00000346607.2:n.72-1489A>T
ENST00000480043.1:n.329+131A>T
NM_001202855.2:c.432+131A>T	NP_001189784.1:n.432+131A>T
NM_017460.5:c.432+131A>T	NP_059488.2:n.432+131A>T
XM_011515841.1:c.432+131A>T	XP_011514143.1:n.432+131A>T
XM_011515842.1:c.432+131A>T	XP_011514144.1:n.432+131A>T
NM_017460.6:c.432+131A>T MANE Select	NP_059488.2:n.432+131A>T
NM_001202855.3:c.432+131A>T	NP_001189784.1:n.432+131A>T