Canonical Allele Identifier: CA1729180196

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767433_99767434delinsAG , CM000669.2:g.99767433_99767434delinsAG	GRCh38
NC_000007.13:g.99365056_99365057delinsAG , CM000669.1:g.99365056_99365057delinsAG	GRCh37
NC_000007.12:g.99202992_99202993delinsAG	NCBI36
NG_008421.1:g.21752_21753delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.671-176_671-175delinsCT	ENSP00000337915.3:n.671-176_671-175delinsCT
ENST00000651162.1:n.106-176_106-175delinsCT
ENST00000651514.1:c.671-176_671-175delinsCT MANE Select	ENSP00000498939.1:n.671-176_671-175delinsCT
ENST00000651783.1:c.212-176_212-175delinsCT	ENSP00000498924.1:n.212-176_212-175delinsCT
ENST00000652018.1:c.524-176_524-175delinsCT	ENSP00000498733.1:n.524-176_524-175delinsCT
ENST00000336411.6:c.671-176_671-175delinsCT	ENSP00000337915.2:n.671-176_671-175delinsCT
ENST00000354593.6:c.221-176_221-175delinsCT	ENSP00000346607.2:n.221-176_221-175delinsCT
NM_001202855.2:c.671-179_671-178delinsCT	NP_001189784.1:n.671-179_671-178delinsCT
NM_017460.5:c.671-176_671-175delinsCT	NP_059488.2:n.671-176_671-175delinsCT
XM_011515841.1:c.671-176_671-175delinsCT	XP_011514143.1:n.671-176_671-175delinsCT
XM_011515842.1:c.671-179_671-178delinsCT	XP_011514144.1:n.671-179_671-178delinsCT
NM_017460.6:c.671-176_671-175delinsCT MANE Select	NP_059488.2:n.671-176_671-175delinsCT
NM_001202855.3:c.671-179_671-178delinsCT	NP_001189784.1:n.671-179_671-178delinsCT