Canonical Allele Identifier: CA2683986053

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99767335-T-TGGTAGAGAAAACTAGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767335_99767336insGGTAGAGAAAACTAGAA , CM000669.2:g.99767335_99767336insGGTAGAGAAAACTAGAA	GRCh38
NC_000007.13:g.99364958_99364959insGGTAGAGAAAACTAGAA , CM000669.1:g.99364958_99364959insGGTAGAGAAAACTAGAA	GRCh37
NC_000007.12:g.99202894_99202895insGGTAGAGAAAACTAGAA	NCBI36
NG_008421.1:g.21850_21851insTTCTAGTTTTCTCTACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.671-78_671-77insTTCTAGTTTTCTCTACC	ENSP00000337915.3:n.671-78_671-77insTTCTAGTTTTCTCTACC
ENST00000651162.1:n.106-78_106-77insTTCTAGTTTTCTCTACC
ENST00000651514.1:c.671-78_671-77insTTCTAGTTTTCTCTACC MANE Select	ENSP00000498939.1:n.671-78_671-77insTTCTAGTTTTCTCTACC
ENST00000651783.1:c.212-78_212-77insTTCTAGTTTTCTCTACC	ENSP00000498924.1:n.212-78_212-77insTTCTAGTTTTCTCTACC
ENST00000652018.1:c.524-78_524-77insTTCTAGTTTTCTCTACC	ENSP00000498733.1:n.524-78_524-77insTTCTAGTTTTCTCTACC
ENST00000336411.6:c.671-78_671-77insTTCTAGTTTTCTCTACC	ENSP00000337915.2:n.671-78_671-77insTTCTAGTTTTCTCTACC
ENST00000354593.6:c.221-78_221-77insTTCTAGTTTTCTCTACC	ENSP00000346607.2:n.221-78_221-77insTTCTAGTTTTCTCTACC
NM_001202855.2:c.671-81_671-80insTTCTAGTTTTCTCTACC	NP_001189784.1:n.671-81_671-80insTTCTAGTTTTCTCTACC
NM_017460.5:c.671-78_671-77insTTCTAGTTTTCTCTACC	NP_059488.2:n.671-78_671-77insTTCTAGTTTTCTCTACC
XM_011515841.1:c.671-78_671-77insTTCTAGTTTTCTCTACC	XP_011514143.1:n.671-78_671-77insTTCTAGTTTTCTCTACC
XM_011515842.1:c.671-81_671-80insTTCTAGTTTTCTCTACC	XP_011514144.1:n.671-81_671-80insTTCTAGTTTTCTCTACC
NM_017460.6:c.671-78_671-77insTTCTAGTTTTCTCTACC MANE Select	NP_059488.2:n.671-78_671-77insTTCTAGTTTTCTCTACC
NM_001202855.3:c.671-81_671-80insTTCTAGTTTTCTCTACC	NP_001189784.1:n.671-81_671-80insTTCTAGTTTTCTCTACC