Canonical Allele Identifier: CA2683985400

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99760950-G-GATC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760951_99760953dup , CM000669.2:g.99760951_99760953dup	GRCh38
NC_000007.13:g.99358574_99358576dup , CM000669.1:g.99358574_99358576dup	GRCh37
NC_000007.12:g.99196510_99196512dup	NCBI36
NG_008421.1:g.28233_28235dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1375_1377dup	ENSP00000337915.3:p.Asp459_Pro460insAsp
ENST00000651162.1:n.717_719dup
ENST00000651514.1:c.1282_1284dup MANE Select	ENSP00000498939.1:p.Asp428_Pro429insAsp
ENST00000651783.1:c.823_825dup	ENSP00000498924.1:p.Asp275_Pro276insAsp
ENST00000652018.1:c.1135_1137dup	ENSP00000498733.1:p.Asp379_Pro380insAsp
ENST00000336411.6:c.1282_1284dup	ENSP00000337915.2:p.Asp428_Pro429insAsp
ENST00000354593.6:c.832_834dup	ENSP00000346607.2:p.Asp278_Pro279insAsp
NM_001202855.2:c.1279_1281dup	NP_001189784.1:p.Asp427_Pro428insAsp
NM_017460.5:c.1282_1284dup	NP_059488.2:p.Asp428_Pro429insAsp
XM_011515841.1:c.1375_1377dup	XP_011514143.1:p.Asp459_Pro460insAsp
XM_011515842.1:c.1372_1374dup	XP_011514144.1:p.Asp458_Pro459insAsp
NM_017460.6:c.1282_1284dup MANE Select	NP_059488.2:p.Asp428_Pro429insAsp
NM_001202855.3:c.1279_1281dup	NP_001189784.1:p.Asp427_Pro428insAsp