Canonical Allele Identifier: CA2546710694
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99760854_99760855insGAGTTCAA , CM000669.2:g.99760854_99760855insGAGTTCAA GRCh38
NC_000007.13:g.99358477_99358478insGAGTTCAA , CM000669.1:g.99358477_99358478insGAGTTCAA GRCh37
NC_000007.12:g.99196413_99196414insGAGTTCAA NCBI36
NG_008421.1:g.28331_28332insTTGAACTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.1473_1474insTTGAACTC ENSP00000337915.3:p.Gln492LeufsTer18
ENST00000651162.1:n.815_816insTTGAACTC
ENST00000651514.1:c.1380_1381insTTGAACTC MANE Select ENSP00000498939.1:p.Gln461LeufsTer18
ENST00000651783.1:c.921_922insTTGAACTC ENSP00000498924.1:p.Gln308LeufsTer18
ENST00000652018.1:c.1233_1234insTTGAACTC ENSP00000498733.1:p.Gln412LeufsTer18
ENST00000336411.6:c.1380_1381insTTGAACTC ENSP00000337915.2:p.Gln461LeufsTer18
ENST00000354593.6:c.930_931insTTGAACTC ENSP00000346607.2:p.Gln311LeufsTer18
NM_001202855.2:c.1377_1378insTTGAACTC NP_001189784.1:p.Gln460LeufsTer18
NM_017460.5:c.1380_1381insTTGAACTC NP_059488.2:p.Gln461LeufsTer18
XM_011515841.1:c.1473_1474insTTGAACTC XP_011514143.1:p.Gln492LeufsTer18
XM_011515842.1:c.1470_1471insTTGAACTC XP_011514144.1:p.Gln491LeufsTer18
NM_017460.6:c.1380_1381insTTGAACTC MANE Select NP_059488.2:p.Gln461LeufsTer18
NM_001202855.3:c.1377_1378insTTGAACTC NP_001189784.1:p.Gln460LeufsTer18