Canonical Allele Identifier: CA1729182092
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99769719_99769722delinsTGGA , CM000669.2:g.99769719_99769722delinsTGGA GRCh38
NC_000007.13:g.99367342_99367345delinsTGGA , CM000669.1:g.99367342_99367345delinsTGGA GRCh37
NC_000007.12:g.99205278_99205281delinsTGGA NCBI36
NG_008421.1:g.19464_19467delinsTCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.521+46_521+49delinsTCCA ENSP00000337915.3:n.521+46_521+49delinsTCCA
ENST00000651514.1:c.521+46_521+49delinsTCCA MANE Select ENSP00000498939.1:n.521+46_521+49delinsTCCA
ENST00000651783.1:c.58-1215_58-1212delinsTCCA ENSP00000498924.1:n.58-1215_58-1212delinsTCCA
ENST00000652018.1:c.374+46_374+49delinsTCCA ENSP00000498733.1:n.374+46_374+49delinsTCCA
ENST00000336411.6:c.521+46_521+49delinsTCCA ENSP00000337915.2:n.521+46_521+49delinsTCCA
ENST00000354593.6:c.72-1220_72-1217delinsTCCA ENSP00000346607.2:n.72-1220_72-1217delinsTCCA
ENST00000480043.1:n.464_467delinsTCCA
NM_001202855.2:c.521+46_521+49delinsTCCA NP_001189784.1:n.521+46_521+49delinsTCCA
NM_017460.5:c.521+46_521+49delinsTCCA NP_059488.2:n.521+46_521+49delinsTCCA
XM_011515841.1:c.521+46_521+49delinsTCCA XP_011514143.1:n.521+46_521+49delinsTCCA
XM_011515842.1:c.521+46_521+49delinsTCCA XP_011514144.1:n.521+46_521+49delinsTCCA
NM_017460.6:c.521+46_521+49delinsTCCA MANE Select NP_059488.2:n.521+46_521+49delinsTCCA
NM_001202855.3:c.521+46_521+49delinsTCCA NP_001189784.1:n.521+46_521+49delinsTCCA