Canonical Allele Identifier: CA1729177313

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762111_99762114delinsTCAC , CM000669.2:g.99762111_99762114delinsTCAC	GRCh38
NC_000007.13:g.99359734_99359737delinsTCAC , CM000669.1:g.99359734_99359737delinsTCAC	GRCh37
NC_000007.12:g.99197670_99197673delinsTCAC	NCBI36
NG_008421.1:g.27072_27075delinsGTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1180_1183delinsGTGA	ENSP00000337915.3:p.Val394=
ENST00000651162.1:n.615_618delinsGTGA
ENST00000651514.1:c.1180_1183delinsGTGA MANE Select	ENSP00000498939.1:p.Val394=
ENST00000651783.1:c.721_724delinsGTGA	ENSP00000498924.1:p.Val241=
ENST00000652018.1:c.1033_1036delinsGTGA	ENSP00000498733.1:p.Val345=
ENST00000336411.6:c.1180_1183delinsGTGA	ENSP00000337915.2:p.Val394=
ENST00000354593.6:c.730_733delinsGTGA	ENSP00000346607.2:p.Val244=
NM_001202855.2:c.1177_1180delinsGTGA	NP_001189784.1:p.Val393=
NM_017460.5:c.1180_1183delinsGTGA	NP_059488.2:p.Val394=
XM_011515841.1:c.1180_1183delinsGTGA	XP_011514143.1:p.Val394=
XM_011515842.1:c.1177_1180delinsGTGA	XP_011514144.1:p.Val393=
NM_017460.6:c.1180_1183delinsGTGA MANE Select	NP_059488.2:p.Val394=
NM_001202855.3:c.1177_1180delinsGTGA	NP_001189784.1:p.Val393=