Canonical Allele Identifier: CA1729180799
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768248_99768249delinsTG , CM000669.2:g.99768248_99768249delinsTG GRCh38
NC_000007.13:g.99365871_99365872delinsTG , CM000669.1:g.99365871_99365872delinsTG GRCh37
NC_000007.12:g.99203807_99203808delinsTG NCBI36
NG_008421.1:g.20937_20938delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.670+105_670+106delinsCA ENSP00000337915.3:n.670+105_670+106delins...
ENST00000651514.1:c.670+105_670+106delinsCA MANE Select ENSP00000498939.1:n.670+105_670+106delins...
ENST00000651783.1:c.211+105_211+106delinsCA ENSP00000498924.1:n.211+105_211+106delins...
ENST00000652018.1:c.523+105_523+106delinsCA ENSP00000498733.1:n.523+105_523+106delins...
ENST00000336411.6:c.670+105_670+106delinsCA ENSP00000337915.2:n.670+105_670+106delins...
ENST00000354593.6:c.220+105_220+106delinsCA ENSP00000346607.2:n.220+105_220+106delins...
NM_001202855.2:c.670+105_670+106delinsCA NP_001189784.1:n.670+105_670+106delinsCA
NM_017460.5:c.670+105_670+106delinsCA NP_059488.2:n.670+105_670+106delinsCA
XM_011515841.1:c.670+105_670+106delinsCA XP_011514143.1:n.670+105_670+106delinsCA
XM_011515842.1:c.670+105_670+106delinsCA XP_011514144.1:n.670+105_670+106delinsCA
NM_017460.6:c.670+105_670+106delinsCA MANE Select NP_059488.2:n.670+105_670+106delinsCA
NM_001202855.3:c.670+105_670+106delinsCA NP_001189784.1:n.670+105_670+106delinsCA