Canonical Allele Identifier: CA2683985802

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99766326-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99766326G>C , CM000669.2:g.99766326G>C	GRCh38
NC_000007.13:g.99363949G>C , CM000669.1:g.99363949G>C	GRCh37
NC_000007.12:g.99201885G>C	NCBI36
NG_008421.1:g.22860C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.865+51C>G	ENSP00000337915.3:n.865+51C>G
ENST00000651162.1:n.300+51C>G
ENST00000651514.1:c.865+51C>G MANE Select	ENSP00000498939.1:n.865+51C>G
ENST00000651783.1:c.406+51C>G	ENSP00000498924.1:n.406+51C>G
ENST00000652018.1:c.718+51C>G	ENSP00000498733.1:n.718+51C>G
ENST00000336411.6:c.865+51C>G	ENSP00000337915.2:n.865+51C>G
ENST00000354593.6:c.415+51C>G	ENSP00000346607.2:n.415+51C>G
NM_001202855.2:c.862+51C>G	NP_001189784.1:n.862+51C>G
NM_017460.5:c.865+51C>G	NP_059488.2:n.865+51C>G
XM_011515841.1:c.865+51C>G	XP_011514143.1:n.865+51C>G
XM_011515842.1:c.862+51C>G	XP_011514144.1:n.862+51C>G
NM_017460.6:c.865+51C>G MANE Select	NP_059488.2:n.865+51C>G
NM_001202855.3:c.862+51C>G	NP_001189784.1:n.862+51C>G