Canonical Allele Identifier: CA2715604225

Gene: CYP3A4

Linked Data

• dbSNP Id: rs2151557399

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99766339_99766340del , CM000669.2:g.99766339_99766340del	GRCh38
NC_000007.13:g.99363962_99363963del , CM000669.1:g.99363962_99363963del	GRCh37
NC_000007.12:g.99201898_99201899del	NCBI36
NG_008421.1:g.22847_22848del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.865+38_865+39del	ENSP00000337915.3:n.865+38_865+39del
ENST00000651162.1:n.300+38_300+39del
ENST00000651514.1:c.865+38_865+39del MANE Select	ENSP00000498939.1:n.865+38_865+39del
ENST00000651783.1:c.406+38_406+39del	ENSP00000498924.1:n.406+38_406+39del
ENST00000652018.1:c.718+38_718+39del	ENSP00000498733.1:n.718+38_718+39del
ENST00000336411.6:c.865+38_865+39del	ENSP00000337915.2:n.865+38_865+39del
ENST00000354593.6:c.415+38_415+39del	ENSP00000346607.2:n.415+38_415+39del
NM_001202855.2:c.862+38_862+39del	NP_001189784.1:n.862+38_862+39del
NM_017460.5:c.865+38_865+39del	NP_059488.2:n.865+38_865+39del
XM_011515841.1:c.865+38_865+39del	XP_011514143.1:n.865+38_865+39del
XM_011515842.1:c.862+38_862+39del	XP_011514144.1:n.862+38_862+39del
NM_017460.6:c.865+38_865+39del MANE Select	NP_059488.2:n.865+38_865+39del
NM_001202855.3:c.862+38_862+39del	NP_001189784.1:n.862+38_862+39del