Canonical Allele Identifier: CA2683986104

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99767400-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767404del , CM000669.2:g.99767404del	GRCh38
NC_000007.13:g.99365027del , CM000669.1:g.99365027del	GRCh37
NC_000007.12:g.99202963del	NCBI36
NG_008421.1:g.21785del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.671-143del	ENSP00000337915.3:n.671-143del
ENST00000651162.1:n.106-143del
ENST00000651514.1:c.671-143del MANE Select	ENSP00000498939.1:n.671-143del
ENST00000651783.1:c.212-143del	ENSP00000498924.1:n.212-143del
ENST00000652018.1:c.524-143del	ENSP00000498733.1:n.524-143del
ENST00000336411.6:c.671-143del	ENSP00000337915.2:n.671-143del
ENST00000354593.6:c.221-143del	ENSP00000346607.2:n.221-143del
NM_001202855.2:c.671-146del	NP_001189784.1:n.671-146del
NM_017460.5:c.671-143del	NP_059488.2:n.671-143del
XM_011515841.1:c.671-143del	XP_011514143.1:n.671-143del
XM_011515842.1:c.671-146del	XP_011514144.1:n.671-146del
NM_017460.6:c.671-143del MANE Select	NP_059488.2:n.671-143del
NM_001202855.3:c.671-146del	NP_001189784.1:n.671-146del