Canonical Allele Identifier: CA2683985957

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99766983-C-CCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99766983_99766984insCAA , CM000669.2:g.99766983_99766984insCAA	GRCh38
NC_000007.13:g.99364606_99364607insCAA , CM000669.1:g.99364606_99364607insCAA	GRCh37
NC_000007.12:g.99202542_99202543insCAA	NCBI36
NG_008421.1:g.22202_22203insTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.798+147_798+148insTTG	ENSP00000337915.3:n.798+147_798+148insTTG
ENST00000651162.1:n.233+147_233+148insTTG
ENST00000651514.1:c.798+147_798+148insTTG MANE Select	ENSP00000498939.1:n.798+147_798+148insTTG
ENST00000651783.1:c.339+147_339+148insTTG	ENSP00000498924.1:n.339+147_339+148insTTG
ENST00000652018.1:c.651+147_651+148insTTG	ENSP00000498733.1:n.651+147_651+148insTTG
ENST00000336411.6:c.798+147_798+148insTTG	ENSP00000337915.2:n.798+147_798+148insTTG
ENST00000354593.6:c.348+147_348+148insTTG	ENSP00000346607.2:n.348+147_348+148insTTG
NM_001202855.2:c.795+147_795+148insTTG	NP_001189784.1:n.795+147_795+148insTTG
NM_017460.5:c.798+147_798+148insTTG	NP_059488.2:n.798+147_798+148insTTG
XM_011515841.1:c.798+147_798+148insTTG	XP_011514143.1:n.798+147_798+148insTTG
XM_011515842.1:c.795+147_795+148insTTG	XP_011514144.1:n.795+147_795+148insTTG
NM_017460.6:c.798+147_798+148insTTG MANE Select	NP_059488.2:n.798+147_798+148insTTG
NM_001202855.3:c.795+147_795+148insTTG	NP_001189784.1:n.795+147_795+148insTTG