Canonical Allele Identifier: CA1104975888

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760992_99760993insGTAGATTTTTTAAAATCTACCAATGTGGATCTATGTTGTCCTTGTTCTTCTTGCTGAATCTGGTTCCACA , CM000669.2:g.99760992_99760993insGTAGATTTTTTAAAATCTACCAATGTGGATCTATGTTGTCCTTGTTCTTCTTGCTGAATCTGGTTCCACA	GRCh38
NC_000007.13:g.99358615_99358616insGTAGATTTTTTAAAATCTACCAATGTGGATCTATGTTGTCCTTGTTCTTCTTGCTGAATCTGGTTCCACA , CM000669.1:g.99358615_99358616insGTAGATTTTTTAAAATCTACCAATGTGGATCTATGTTGTCCTTGTTCTTCTTGCTGAATCTGGTTCCACA	GRCh37
NC_000007.12:g.99196551_99196552insGTAGATTTTTTAAAATCTACCAATGTGGATCTATGTTGTCCTTGTTCTTCTTGCTGAATCTGGTTCCACA	NCBI36
NG_008421.1:g.28193_28194insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1347-12_1347-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC	ENSP00000337915.3:n.1347-12_1347-11insTGTGGAACCAGATTCAGCAAGAA...
ENST00000651162.1:n.689-12_689-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC
ENST00000651514.1:c.1254-12_1254-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC MANE Select	ENSP00000498939.1:n.1254-12_1254-11insTGTGGAACCAGATTCAGCAAGAA...
ENST00000651783.1:c.795-12_795-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC	ENSP00000498924.1:n.795-12_795-11insTGTGGAACCAGATTCAGCAAGAAGA...
ENST00000652018.1:c.1107-12_1107-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC	ENSP00000498733.1:n.1107-12_1107-11insTGTGGAACCAGATTCAGCAAGAA...
ENST00000336411.6:c.1254-12_1254-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC	ENSP00000337915.2:n.1254-12_1254-11insTGTGGAACCAGATTCAGCAAGAA...
ENST00000354593.6:c.804-12_804-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC	ENSP00000346607.2:n.804-12_804-11insTGTGGAACCAGATTCAGCAAGAAGA...
NM_001202855.2:c.1251-12_1251-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC	NP_001189784.1:n.1251-12_1251-11insTGTGGAACCAGATTCAGCAAGAAGAA...
NM_017460.5:c.1254-12_1254-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC	NP_059488.2:n.1254-12_1254-11insTGTGGAACCAGATTCAGCAAGAAGAACAA...
XM_011515841.1:c.1347-12_1347-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC	XP_011514143.1:n.1347-12_1347-11insTGTGGAACCAGATTCAGCAAGAAGAA...
XM_011515842.1:c.1344-12_1344-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC	XP_011514144.1:n.1344-12_1344-11insTGTGGAACCAGATTCAGCAAGAAGAA...
NM_017460.6:c.1254-12_1254-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC MANE Select	NP_059488.2:n.1254-12_1254-11insTGTGGAACCAGATTCAGCAAGAAGAACAA...
NM_001202855.3:c.1251-12_1251-11insTGTGGAACCAGATTCAGCAAGAAGAACAAGGACAACATAGATCCACATTGGTAGATTTTAAAAAATCTAC	NP_001189784.1:n.1251-12_1251-11insTGTGGAACCAGATTCAGCAAGAAGAA...