Canonical Allele Identifier: CA1729180844
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768338_99768341delinsATAG , CM000669.2:g.99768338_99768341delinsATAG GRCh38
NC_000007.13:g.99365961_99365964delinsATAG , CM000669.1:g.99365961_99365964delinsATAG GRCh37
NC_000007.12:g.99203897_99203900delinsATAG NCBI36
NG_008421.1:g.20845_20848delinsCTAT

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.670+13_670+16delinsCTAT ENSP00000337915.3:n.670+13_670+16delinsCT...
ENST00000651514.1:c.670+13_670+16delinsCTAT MANE Select ENSP00000498939.1:n.670+13_670+16delinsCT...
ENST00000651783.1:c.211+13_211+16delinsCTAT ENSP00000498924.1:n.211+13_211+16delinsCT...
ENST00000652018.1:c.523+13_523+16delinsCTAT ENSP00000498733.1:n.523+13_523+16delinsCT...
ENST00000336411.6:c.670+13_670+16delinsCTAT ENSP00000337915.2:n.670+13_670+16delinsCT...
ENST00000354593.6:c.220+13_220+16delinsCTAT ENSP00000346607.2:n.220+13_220+16delinsCT...
NM_001202855.2:c.670+13_670+16delinsCTAT NP_001189784.1:n.670+13_670+16delinsCTAT
NM_017460.5:c.670+13_670+16delinsCTAT NP_059488.2:n.670+13_670+16delinsCTAT
XM_011515841.1:c.670+13_670+16delinsCTAT XP_011514143.1:n.670+13_670+16delinsCTAT
XM_011515842.1:c.670+13_670+16delinsCTAT XP_011514144.1:n.670+13_670+16delinsCTAT
NM_017460.6:c.670+13_670+16delinsCTAT MANE Select NP_059488.2:n.670+13_670+16delinsCTAT
NM_001202855.3:c.670+13_670+16delinsCTAT NP_001189784.1:n.670+13_670+16delinsCTAT