Canonical Allele Identifier: CA1729181732

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769347_99769348delinsTG , CM000669.2:g.99769347_99769348delinsTG	GRCh38
NC_000007.13:g.99366970_99366971delinsTG , CM000669.1:g.99366970_99366971delinsTG	GRCh37
NC_000007.12:g.99204906_99204907delinsTG	NCBI36
NG_008421.1:g.19838_19839delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+420_521+421delinsCA	ENSP00000337915.3:n.521+420_521+421delinsCA
ENST00000651514.1:c.521+420_521+421delinsCA MANE Select	ENSP00000498939.1:n.521+420_521+421delinsCA
ENST00000651783.1:c.58-841_58-840delinsCA	ENSP00000498924.1:n.58-841_58-840delinsCA
ENST00000652018.1:c.374+420_374+421delinsCA	ENSP00000498733.1:n.374+420_374+421delinsCA
ENST00000336411.6:c.521+420_521+421delinsCA	ENSP00000337915.2:n.521+420_521+421delinsCA
ENST00000354593.6:c.72-846_72-845delinsCA	ENSP00000346607.2:n.72-846_72-845delinsCA
NM_001202855.2:c.521+420_521+421delinsCA	NP_001189784.1:n.521+420_521+421delinsCA
NM_017460.5:c.521+420_521+421delinsCA	NP_059488.2:n.521+420_521+421delinsCA
XM_011515841.1:c.521+420_521+421delinsCA	XP_011514143.1:n.521+420_521+421delinsCA
XM_011515842.1:c.521+420_521+421delinsCA	XP_011514144.1:n.521+420_521+421delinsCA
NM_017460.6:c.521+420_521+421delinsCA MANE Select	NP_059488.2:n.521+420_521+421delinsCA
NM_001202855.3:c.521+420_521+421delinsCA	NP_001189784.1:n.521+420_521+421delinsCA