Canonical Allele Identifier: CA4369510

Gene: CYP3A4

Linked Data

• dbSNP Id: rs771694686
• ExAC: 7:99358583 G / A
• gnomAD v2: 7-99358583-G-A
• gnomAD v4: 7-99760960-G-A
• MyVariant Identifiers: chr7:g.99358583G>A (hg19) ; chr7:g.99760960G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760960G>A , CM000669.2:g.99760960G>A	GRCh38
NC_000007.13:g.99358583G>A , CM000669.1:g.99358583G>A	GRCh37
NC_000007.12:g.99196519G>A	NCBI36
NG_008421.1:g.28226C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1368C>T	ENSP00000337915.3:p.Asp456=
ENST00000651162.1:n.710C>T
ENST00000651514.1:c.1275C>T MANE Select	ENSP00000498939.1:p.Asp425=
ENST00000651783.1:c.816C>T	ENSP00000498924.1:p.Asp272=
ENST00000652018.1:c.1128C>T	ENSP00000498733.1:p.Asp376=
ENST00000336411.6:c.1275C>T	ENSP00000337915.2:p.Asp425=
ENST00000354593.6:c.825C>T	ENSP00000346607.2:p.Asp275=
NM_001202855.2:c.1272C>T	NP_001189784.1:p.Asp424=
NM_017460.5:c.1275C>T	NP_059488.2:p.Asp425=
XM_011515841.1:c.1368C>T	XP_011514143.1:p.Asp456=
XM_011515842.1:c.1365C>T	XP_011514144.1:p.Asp455=
NM_017460.6:c.1275C>T MANE Select	NP_059488.2:p.Asp425=
NM_001202855.3:c.1272C>T	NP_001189784.1:p.Asp424=