Canonical Allele Identifier: CA576400238

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1396698651
• gnomAD v2: 7-99358446-GTTTC-G
• MyVariant Identifiers: chr7:g.99358447_99358450del (hg19) ; chr7:g.99760824_99760827del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760827_99760830del , CM000669.2:g.99760827_99760830del	GRCh38
NC_000007.13:g.99358450_99358453del , CM000669.1:g.99358450_99358453del	GRCh37
NC_000007.12:g.99196386_99196389del	NCBI36
NG_008421.1:g.28359_28362del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1501_1504del	ENSP00000337915.3:p.Glu501HisfsTer5
ENST00000651162.1:n.843_846del
ENST00000651514.1:c.1408_1411del MANE Select	ENSP00000498939.1:p.Glu470HisfsTer5
ENST00000651783.1:c.949_952del	ENSP00000498924.1:p.Glu317HisfsTer5
ENST00000652018.1:c.1261_1264del	ENSP00000498733.1:p.Glu421HisfsTer5
ENST00000336411.6:c.1408_1411del	ENSP00000337915.2:p.Glu470HisfsTer5
ENST00000354593.6:c.958_961del	ENSP00000346607.2:p.Glu320HisfsTer5
NM_001202855.2:c.1405_1408del	NP_001189784.1:p.Glu469HisfsTer5
NM_017460.5:c.1408_1411del	NP_059488.2:p.Glu470HisfsTer5
XM_011515841.1:c.1501_1504del	XP_011514143.1:p.Glu501HisfsTer5
XM_011515842.1:c.1498_1501del	XP_011514144.1:p.Glu500HisfsTer5
NM_017460.6:c.1408_1411del MANE Select	NP_059488.2:p.Glu470HisfsTer5
NM_001202855.3:c.1405_1408del	NP_001189784.1:p.Glu469HisfsTer5