Canonical Allele Identifier: CA576401751

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1485724878
• gnomAD v2: 7-99364738-TACC-T
• gnomAD v4: 7-99767115-TACC-T
• MyVariant Identifiers: chr7:g.99364739_99364741del (hg19) ; chr7:g.99767116_99767118del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767121_99767123del , CM000669.2:g.99767121_99767123del	GRCh38
NC_000007.13:g.99364744_99364746del , CM000669.1:g.99364744_99364746del	GRCh37
NC_000007.12:g.99202680_99202682del	NCBI36
NG_008421.1:g.22068_22070del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.798+13_798+15del	ENSP00000337915.3:n.798+13_798+15del
ENST00000651162.1:n.233+13_233+15del
ENST00000651514.1:c.798+13_798+15del MANE Select	ENSP00000498939.1:n.798+13_798+15del
ENST00000651783.1:c.339+13_339+15del	ENSP00000498924.1:n.339+13_339+15del
ENST00000652018.1:c.651+13_651+15del	ENSP00000498733.1:n.651+13_651+15del
ENST00000336411.6:c.798+13_798+15del	ENSP00000337915.2:n.798+13_798+15del
ENST00000354593.6:c.348+13_348+15del	ENSP00000346607.2:n.348+13_348+15del
NM_001202855.2:c.795+13_795+15del	NP_001189784.1:n.795+13_795+15del
NM_017460.5:c.798+13_798+15del	NP_059488.2:n.798+13_798+15del
XM_011515841.1:c.798+13_798+15del	XP_011514143.1:n.798+13_798+15del
XM_011515842.1:c.795+13_795+15del	XP_011514144.1:n.795+13_795+15del
NM_017460.6:c.798+13_798+15del MANE Select	NP_059488.2:n.798+13_798+15del
NM_001202855.3:c.795+13_795+15del	NP_001189784.1:n.795+13_795+15del