Canonical Allele Identifier: CA1729180855

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815528378

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768357_99768362del , CM000669.2:g.99768357_99768362del	GRCh38
NC_000007.13:g.99365980_99365985del , CM000669.1:g.99365980_99365985del	GRCh37
NC_000007.12:g.99203916_99203921del	NCBI36
NG_008421.1:g.20825_20830del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.663_668del	ENSP00000337915.3:p.Ser222_Ile223del
ENST00000651514.1:c.663_668del MANE Select	ENSP00000498939.1:p.Ser222_Ile223del
ENST00000651783.1:c.204_209del	ENSP00000498924.1:p.Ser69_Ile70del
ENST00000652018.1:c.516_521del	ENSP00000498733.1:p.Ser173_Ile174del
ENST00000336411.6:c.663_668del	ENSP00000337915.2:p.Ser222_Ile223del
ENST00000354593.6:c.213_218del	ENSP00000346607.2:p.Ser72_Ile73del
NM_001202855.2:c.663_668del	NP_001189784.1:p.Ser222_Ile223del
NM_017460.5:c.663_668del	NP_059488.2:p.Ser222_Ile223del
XM_011515841.1:c.663_668del	XP_011514143.1:p.Ser222_Ile223del
XM_011515842.1:c.663_668del	XP_011514144.1:p.Ser222_Ile223del
NM_017460.6:c.663_668del MANE Select	NP_059488.2:p.Ser222_Ile223del
NM_001202855.3:c.663_668del	NP_001189784.1:p.Ser222_Ile223del