Canonical Allele Identifier: CA2683986180
Gene: CYP3A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768317_99768320del , CM000669.2:g.99768317_99768320del GRCh38
NC_000007.13:g.99365940_99365943del , CM000669.1:g.99365940_99365943del GRCh37
NC_000007.12:g.99203876_99203879del NCBI36
NG_008421.1:g.20866_20869del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.670+34_670+37del ENSP00000337915.3:n.670+34_670+37del
ENST00000651514.1:c.670+34_670+37del MANE Select ENSP00000498939.1:n.670+34_670+37del
ENST00000651783.1:c.211+34_211+37del ENSP00000498924.1:n.211+34_211+37del
ENST00000652018.1:c.523+34_523+37del ENSP00000498733.1:n.523+34_523+37del
ENST00000336411.6:c.670+34_670+37del ENSP00000337915.2:n.670+34_670+37del
ENST00000354593.6:c.220+34_220+37del ENSP00000346607.2:n.220+34_220+37del
NM_001202855.2:c.670+34_670+37del NP_001189784.1:n.670+34_670+37del
NM_017460.5:c.670+34_670+37del NP_059488.2:n.670+34_670+37del
XM_011515841.1:c.670+34_670+37del XP_011514143.1:n.670+34_670+37del
XM_011515842.1:c.670+34_670+37del XP_011514144.1:n.670+34_670+37del
NM_017460.6:c.670+34_670+37del MANE Select NP_059488.2:n.670+34_670+37del
NM_001202855.3:c.670+34_670+37del NP_001189784.1:n.670+34_670+37del