Canonical Allele Identifier: CA2683986445

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99769665-GTCTGGTCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769666_99769673del , CM000669.2:g.99769666_99769673del	GRCh38
NC_000007.13:g.99367289_99367296del , CM000669.1:g.99367289_99367296del	GRCh37
NC_000007.12:g.99205225_99205232del	NCBI36
NG_008421.1:g.19513_19520del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+95_521+102del	ENSP00000337915.3:n.521+95_521+102del
ENST00000651514.1:c.521+95_521+102del MANE Select	ENSP00000498939.1:n.521+95_521+102del
ENST00000651783.1:c.58-1166_58-1159del	ENSP00000498924.1:n.58-1166_58-1159del
ENST00000652018.1:c.374+95_374+102del	ENSP00000498733.1:n.374+95_374+102del
ENST00000336411.6:c.521+95_521+102del	ENSP00000337915.2:n.521+95_521+102del
ENST00000354593.6:c.72-1171_72-1164del	ENSP00000346607.2:n.72-1171_72-1164del
ENST00000480043.1:n.513_520del
NM_001202855.2:c.521+95_521+102del	NP_001189784.1:n.521+95_521+102del
NM_017460.5:c.521+95_521+102del	NP_059488.2:n.521+95_521+102del
XM_011515841.1:c.521+95_521+102del	XP_011514143.1:n.521+95_521+102del
XM_011515842.1:c.521+95_521+102del	XP_011514144.1:n.521+95_521+102del
NM_017460.6:c.521+95_521+102del MANE Select	NP_059488.2:n.521+95_521+102del
NM_001202855.3:c.521+95_521+102del	NP_001189784.1:n.521+95_521+102del