Canonical Allele Identifier: CA1729176739

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760841_99760844delinsAAGG , CM000669.2:g.99760841_99760844delinsAAGG	GRCh38
NC_000007.13:g.99358464_99358467delinsAAGG , CM000669.1:g.99358464_99358467delinsAAGG	GRCh37
NC_000007.12:g.99196400_99196403delinsAAGG	NCBI36
NG_008421.1:g.28342_28345delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1484_1487delinsCCTT	ENSP00000337915.3:p.Ser495=
ENST00000651162.1:n.826_829delinsCCTT
ENST00000651514.1:c.1391_1394delinsCCTT MANE Select	ENSP00000498939.1:p.Ser464=
ENST00000651783.1:c.932_935delinsCCTT	ENSP00000498924.1:p.Ser311=
ENST00000652018.1:c.1244_1247delinsCCTT	ENSP00000498733.1:p.Ser415=
ENST00000336411.6:c.1391_1394delinsCCTT	ENSP00000337915.2:p.Ser464=
ENST00000354593.6:c.941_944delinsCCTT	ENSP00000346607.2:p.Ser314=
NM_001202855.2:c.1388_1391delinsCCTT	NP_001189784.1:p.Ser463=
NM_017460.5:c.1391_1394delinsCCTT	NP_059488.2:p.Ser464=
XM_011515841.1:c.1484_1487delinsCCTT	XP_011514143.1:p.Ser495=
XM_011515842.1:c.1481_1484delinsCCTT	XP_011514144.1:p.Ser494=
NM_017460.6:c.1391_1394delinsCCTT MANE Select	NP_059488.2:p.Ser464=
NM_001202855.3:c.1388_1391delinsCCTT	NP_001189784.1:p.Ser463=