Canonical Allele Identifier: CA1729180913

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768435_99768439delinsTGAGA , CM000669.2:g.99768435_99768439delinsTGAGA	GRCh38
NC_000007.13:g.99366058_99366062delinsTGAGA , CM000669.1:g.99366058_99366062delinsTGAGA	GRCh37
NC_000007.12:g.99203994_99203998delinsTGAGA	NCBI36
NG_008421.1:g.20747_20751delinsTCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.585_589delinsTCTCA	ENSP00000337915.3:p.Ser195=
ENST00000651514.1:c.585_589delinsTCTCA MANE Select	ENSP00000498939.1:p.Ser195=
ENST00000651783.1:c.126_130delinsTCTCA	ENSP00000498924.1:p.Ser42=
ENST00000652018.1:c.438_442delinsTCTCA	ENSP00000498733.1:p.Ser146=
ENST00000336411.6:c.585_589delinsTCTCA	ENSP00000337915.2:p.Ser195=
ENST00000354593.6:c.135_139delinsTCTCA	ENSP00000346607.2:p.Ser45=
NM_001202855.2:c.585_589delinsTCTCA	NP_001189784.1:p.Ser195=
NM_017460.5:c.585_589delinsTCTCA	NP_059488.2:p.Ser195=
XM_011515841.1:c.585_589delinsTCTCA	XP_011514143.1:p.Ser195=
XM_011515842.1:c.585_589delinsTCTCA	XP_011514144.1:p.Ser195=
NM_017460.6:c.585_589delinsTCTCA MANE Select	NP_059488.2:p.Ser195=
NM_001202855.3:c.585_589delinsTCTCA	NP_001189784.1:p.Ser195=