Canonical Allele Identifier: CA2777115391

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767005del , CM000669.2:g.99767005del	GRCh38
NC_000007.13:g.99364628del , CM000669.1:g.99364628del	GRCh37
NC_000007.12:g.99202564del	NCBI36
NG_008421.1:g.22183del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.798+128del	ENSP00000337915.3:n.798+128del
ENST00000651162.1:n.233+128del
ENST00000651514.1:c.798+128del MANE Select	ENSP00000498939.1:n.798+128del
ENST00000651783.1:c.339+128del	ENSP00000498924.1:n.339+128del
ENST00000652018.1:c.651+128del	ENSP00000498733.1:n.651+128del
ENST00000336411.6:c.798+128del	ENSP00000337915.2:n.798+128del
ENST00000354593.6:c.348+128del	ENSP00000346607.2:n.348+128del
NM_001202855.2:c.795+128del	NP_001189784.1:n.795+128del
NM_017460.5:c.798+128del	NP_059488.2:n.798+128del
XM_011515841.1:c.798+128del	XP_011514143.1:n.798+128del
XM_011515842.1:c.795+128del	XP_011514144.1:n.795+128del
NM_017460.6:c.798+128del MANE Select	NP_059488.2:n.798+128del
NM_001202855.3:c.795+128del	NP_001189784.1:n.795+128del