Canonical Allele Identifier: CA1729176654

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760622_99760625delinsCATG , CM000669.2:g.99760622_99760625delinsCATG	GRCh38
NC_000007.13:g.99358245_99358248delinsCATG , CM000669.1:g.99358245_99358248delinsCATG	GRCh37
NC_000007.12:g.99196181_99196184delinsCATG	NCBI36
NG_008421.1:g.28561_28564delinsCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1509+194_1509+197delinsCATG	ENSP00000337915.3:n.1509+194_1509+197delinsCATG
ENST00000651162.1:n.851+194_851+197delinsCATG
ENST00000651514.1:c.1416+194_1416+197delinsCATG MANE Select	ENSP00000498939.1:n.1416+194_1416+197delinsCATG
ENST00000651783.1:c.957+194_957+197delinsCATG	ENSP00000498924.1:n.957+194_957+197delinsCATG
ENST00000652018.1:c.1269+194_1269+197delinsCATG	ENSP00000498733.1:n.1269+194_1269+197delinsCATG
ENST00000336411.6:c.1416+194_1416+197delinsCATG	ENSP00000337915.2:n.1416+194_1416+197delinsCATG
ENST00000354593.6:c.966+194_966+197delinsCATG	ENSP00000346607.2:n.966+194_966+197delinsCATG
NM_001202855.2:c.1413+194_1413+197delinsCATG	NP_001189784.1:n.1413+194_1413+197delinsCATG
NM_017460.5:c.1416+194_1416+197delinsCATG	NP_059488.2:n.1416+194_1416+197delinsCATG
XM_011515841.1:c.1509+194_1509+197delinsCATG	XP_011514143.1:n.1509+194_1509+197delinsCATG
XM_011515842.1:c.1506+194_1506+197delinsCATG	XP_011514144.1:n.1506+194_1506+197delinsCATG
NM_017460.6:c.1416+194_1416+197delinsCATG MANE Select	NP_059488.2:n.1416+194_1416+197delinsCATG
NM_001202855.3:c.1413+194_1413+197delinsCATG	NP_001189784.1:n.1413+194_1413+197delinsCATG