Canonical Allele Identifier: CA4369749

Gene: CYP3A4

Linked Data

• dbSNP Id: rs778287319
• ExAC: 7:99367448 A / G
• gnomAD v2: 7-99367448-A-G
• gnomAD v4: 7-99769825-A-G
• MyVariant Identifiers: chr7:g.99367448A>G (hg19) ; chr7:g.99769825A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769825A>G , CM000669.2:g.99769825A>G	GRCh38
NC_000007.13:g.99367448A>G , CM000669.1:g.99367448A>G	GRCh37
NC_000007.12:g.99205384A>G	NCBI36
NG_008421.1:g.19361T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.464T>C	ENSP00000337915.3:p.Val155Ala
ENST00000651514.1:c.464T>C MANE Select	ENSP00000498939.1:p.Val155Ala
ENST00000651783.1:c.58-1318T>C	ENSP00000498924.1:n.58-1318T>C
ENST00000652018.1:c.317T>C	ENSP00000498733.1:p.Val106Ala
ENST00000336411.6:c.464T>C	ENSP00000337915.2:p.Val155Ala
ENST00000354593.6:c.72-1323T>C	ENSP00000346607.2:n.72-1323T>C
ENST00000480043.1:n.361T>C
NM_001202855.2:c.464T>C	NP_001189784.1:p.Val155Ala
NM_017460.5:c.464T>C	NP_059488.2:p.Val155Ala
XM_011515841.1:c.464T>C	XP_011514143.1:p.Val155Ala
XM_011515842.1:c.464T>C	XP_011514144.1:p.Val155Ala
NM_017460.6:c.464T>C MANE Select	NP_059488.2:p.Val155Ala
NM_001202855.3:c.464T>C	NP_001189784.1:p.Val155Ala