Canonical Allele Identifier: CA2777115424

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767494_99767495insACA , CM000669.2:g.99767494_99767495insACA	GRCh38
NC_000007.13:g.99365117_99365118insACA , CM000669.1:g.99365117_99365118insACA	GRCh37
NC_000007.12:g.99203053_99203054insACA	NCBI36
NG_008421.1:g.21691_21692insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.671-237_671-236insTGT	ENSP00000337915.3:n.671-237_671-236insTGT
ENST00000651162.1:n.105+223_105+224insTGT
ENST00000651514.1:c.671-237_671-236insTGT MANE Select	ENSP00000498939.1:n.671-237_671-236insTGT
ENST00000651783.1:c.212-237_212-236insTGT	ENSP00000498924.1:n.212-237_212-236insTGT
ENST00000652018.1:c.524-237_524-236insTGT	ENSP00000498733.1:n.524-237_524-236insTGT
ENST00000336411.6:c.671-237_671-236insTGT	ENSP00000337915.2:n.671-237_671-236insTGT
ENST00000354593.6:c.221-237_221-236insTGT	ENSP00000346607.2:n.221-237_221-236insTGT
NM_001202855.2:c.671-240_671-239insTGT	NP_001189784.1:n.671-240_671-239insTGT
NM_017460.5:c.671-237_671-236insTGT	NP_059488.2:n.671-237_671-236insTGT
XM_011515841.1:c.671-237_671-236insTGT	XP_011514143.1:n.671-237_671-236insTGT
XM_011515842.1:c.671-240_671-239insTGT	XP_011514144.1:n.671-240_671-239insTGT
NM_017460.6:c.671-237_671-236insTGT MANE Select	NP_059488.2:n.671-237_671-236insTGT
NM_001202855.3:c.671-240_671-239insTGT	NP_001189784.1:n.671-240_671-239insTGT