Canonical Allele Identifier: CA368368678

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1384173693
• gnomAD v2: 7-99358561-T-C
• gnomAD v4: 7-99760938-T-C
• MyVariant Identifiers: chr7:g.99358561T>C (hg19) ; chr7:g.99760938T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760938T>C , CM000669.2:g.99760938T>C	GRCh38
NC_000007.13:g.99358561T>C , CM000669.1:g.99358561T>C	GRCh37
NC_000007.12:g.99196497T>C	NCBI36
NG_008421.1:g.28248A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1390A>G	ENSP00000337915.3:p.Thr464Ala
ENST00000651162.1:n.732A>G
ENST00000651514.1:c.1297A>G MANE Select	ENSP00000498939.1:p.Thr433Ala
ENST00000651783.1:c.838A>G	ENSP00000498924.1:p.Thr280Ala
ENST00000652018.1:c.1150A>G	ENSP00000498733.1:p.Thr384Ala
ENST00000336411.6:c.1297A>G	ENSP00000337915.2:p.Thr433Ala
ENST00000354593.6:c.847A>G	ENSP00000346607.2:p.Thr283Ala
NM_001202855.2:c.1294A>G	NP_001189784.1:p.Thr432Ala
NM_017460.5:c.1297A>G	NP_059488.2:p.Thr433Ala
XM_011515841.1:c.1390A>G	XP_011514143.1:p.Thr464Ala
XM_011515842.1:c.1387A>G	XP_011514144.1:p.Thr463Ala
NM_017460.6:c.1297A>G MANE Select	NP_059488.2:p.Thr433Ala
NM_001202855.3:c.1294A>G	NP_001189784.1:p.Thr432Ala