Canonical Allele Identifier: CA2777115531

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769673_99769674insG , CM000669.2:g.99769673_99769674insG	GRCh38
NC_000007.13:g.99367296_99367297insG , CM000669.1:g.99367296_99367297insG	GRCh37
NC_000007.12:g.99205232_99205233insG	NCBI36
NG_008421.1:g.19512_19513insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+94_521+95insC	ENSP00000337915.3:n.521+94_521+95insC
ENST00000651514.1:c.521+94_521+95insC MANE Select	ENSP00000498939.1:n.521+94_521+95insC
ENST00000651783.1:c.58-1167_58-1166insC	ENSP00000498924.1:n.58-1167_58-1166insC
ENST00000652018.1:c.374+94_374+95insC	ENSP00000498733.1:n.374+94_374+95insC
ENST00000336411.6:c.521+94_521+95insC	ENSP00000337915.2:n.521+94_521+95insC
ENST00000354593.6:c.72-1172_72-1171insC	ENSP00000346607.2:n.72-1172_72-1171insC
ENST00000480043.1:n.512_513insC
NM_001202855.2:c.521+94_521+95insC	NP_001189784.1:n.521+94_521+95insC
NM_017460.5:c.521+94_521+95insC	NP_059488.2:n.521+94_521+95insC
XM_011515841.1:c.521+94_521+95insC	XP_011514143.1:n.521+94_521+95insC
XM_011515842.1:c.521+94_521+95insC	XP_011514144.1:n.521+94_521+95insC
NM_017460.6:c.521+94_521+95insC MANE Select	NP_059488.2:n.521+94_521+95insC
NM_001202855.3:c.521+94_521+95insC	NP_001189784.1:n.521+94_521+95insC