Canonical Allele Identifier: CA1729179949

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767152_99767156delinsACTTT , CM000669.2:g.99767152_99767156delinsACTTT	GRCh38
NC_000007.13:g.99364775_99364779delinsACTTT , CM000669.1:g.99364775_99364779delinsACTTT	GRCh37
NC_000007.12:g.99202711_99202715delinsACTTT	NCBI36
NG_008421.1:g.22030_22034delinsAAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.773_777delinsAAAGT	ENSP00000337915.3:p.Glu258=
ENST00000651162.1:n.208_212delinsAAAGT
ENST00000651514.1:c.773_777delinsAAAGT MANE Select	ENSP00000498939.1:p.Glu258=
ENST00000651783.1:c.314_318delinsAAAGT	ENSP00000498924.1:p.Glu105=
ENST00000652018.1:c.626_630delinsAAAGT	ENSP00000498733.1:p.Glu209=
ENST00000336411.6:c.773_777delinsAAAGT	ENSP00000337915.2:p.Glu258=
ENST00000354593.6:c.323_327delinsAAAGT	ENSP00000346607.2:p.Glu108=
NM_001202855.2:c.770_774delinsAAAGT	NP_001189784.1:p.Glu257=
NM_017460.5:c.773_777delinsAAAGT	NP_059488.2:p.Glu258=
XM_011515841.1:c.773_777delinsAAAGT	XP_011514143.1:p.Glu258=
XM_011515842.1:c.770_774delinsAAAGT	XP_011514144.1:p.Glu257=
NM_017460.6:c.773_777delinsAAAGT MANE Select	NP_059488.2:p.Glu258=
NM_001202855.3:c.770_774delinsAAAGT	NP_001189784.1:p.Glu257=