Canonical Allele Identifier: CA2578955141

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99766333-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99766336_99766337del , CM000669.2:g.99766336_99766337del	GRCh38
NC_000007.13:g.99363959_99363960del , CM000669.1:g.99363959_99363960del	GRCh37
NC_000007.12:g.99201895_99201896del	NCBI36
NG_008421.1:g.22851_22852del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.865+42_865+43del	ENSP00000337915.3:n.865+42_865+43del
ENST00000651162.1:n.300+42_300+43del
ENST00000651514.1:c.865+42_865+43del MANE Select	ENSP00000498939.1:n.865+42_865+43del
ENST00000651783.1:c.406+42_406+43del	ENSP00000498924.1:n.406+42_406+43del
ENST00000652018.1:c.718+42_718+43del	ENSP00000498733.1:n.718+42_718+43del
ENST00000336411.6:c.865+42_865+43del	ENSP00000337915.2:n.865+42_865+43del
ENST00000354593.6:c.415+42_415+43del	ENSP00000346607.2:n.415+42_415+43del
NM_001202855.2:c.862+42_862+43del	NP_001189784.1:n.862+42_862+43del
NM_017460.5:c.865+42_865+43del	NP_059488.2:n.865+42_865+43del
XM_011515841.1:c.865+42_865+43del	XP_011514143.1:n.865+42_865+43del
XM_011515842.1:c.862+42_862+43del	XP_011514144.1:n.862+42_862+43del
NM_017460.6:c.865+42_865+43del MANE Select	NP_059488.2:n.865+42_865+43del
NM_001202855.3:c.862+42_862+43del	NP_001189784.1:n.862+42_862+43del