Canonical Allele Identifier: CA2683986175

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99768304-G-GTTATTT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768308_99768313dup , CM000669.2:g.99768308_99768313dup	GRCh38
NC_000007.13:g.99365931_99365936dup , CM000669.1:g.99365931_99365936dup	GRCh37
NC_000007.12:g.99203867_99203872dup	NCBI36
NG_008421.1:g.20876_20881dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.670+44_670+49dup	ENSP00000337915.3:n.670+44_670+49dup
ENST00000651514.1:c.670+44_670+49dup MANE Select	ENSP00000498939.1:n.670+44_670+49dup
ENST00000651783.1:c.211+44_211+49dup	ENSP00000498924.1:n.211+44_211+49dup
ENST00000652018.1:c.523+44_523+49dup	ENSP00000498733.1:n.523+44_523+49dup
ENST00000336411.6:c.670+44_670+49dup	ENSP00000337915.2:n.670+44_670+49dup
ENST00000354593.6:c.220+44_220+49dup	ENSP00000346607.2:n.220+44_220+49dup
NM_001202855.2:c.670+44_670+49dup	NP_001189784.1:n.670+44_670+49dup
NM_017460.5:c.670+44_670+49dup	NP_059488.2:n.670+44_670+49dup
XM_011515841.1:c.670+44_670+49dup	XP_011514143.1:n.670+44_670+49dup
XM_011515842.1:c.670+44_670+49dup	XP_011514144.1:n.670+44_670+49dup
NM_017460.6:c.670+44_670+49dup MANE Select	NP_059488.2:n.670+44_670+49dup
NM_001202855.3:c.670+44_670+49dup	NP_001189784.1:n.670+44_670+49dup