Canonical Allele Identifier: CA1729179282
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99766329_99766330delinsCT , CM000669.2:g.99766329_99766330delinsCT GRCh38
NC_000007.13:g.99363952_99363953delinsCT , CM000669.1:g.99363952_99363953delinsCT GRCh37
NC_000007.12:g.99201888_99201889delinsCT NCBI36
NG_008421.1:g.22856_22857delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.865+47_865+48delinsAG ENSP00000337915.3:n.865+47_865+48delinsAG...
ENST00000651162.1:n.300+47_300+48delinsAG
ENST00000651514.1:c.865+47_865+48delinsAG MANE Select ENSP00000498939.1:n.865+47_865+48delinsAG...
ENST00000651783.1:c.406+47_406+48delinsAG ENSP00000498924.1:n.406+47_406+48delinsAG...
ENST00000652018.1:c.718+47_718+48delinsAG ENSP00000498733.1:n.718+47_718+48delinsAG...
ENST00000336411.6:c.865+47_865+48delinsAG ENSP00000337915.2:n.865+47_865+48delinsAG...
ENST00000354593.6:c.415+47_415+48delinsAG ENSP00000346607.2:n.415+47_415+48delinsAG...
NM_001202855.2:c.862+47_862+48delinsAG NP_001189784.1:n.862+47_862+48delinsAG
NM_017460.5:c.865+47_865+48delinsAG NP_059488.2:n.865+47_865+48delinsAG
XM_011515841.1:c.865+47_865+48delinsAG XP_011514143.1:n.865+47_865+48delinsAG
XM_011515842.1:c.862+47_862+48delinsAG XP_011514144.1:n.862+47_862+48delinsAG
NM_017460.6:c.865+47_865+48delinsAG MANE Select NP_059488.2:n.865+47_865+48delinsAG
NM_001202855.3:c.862+47_862+48delinsAG NP_001189784.1:n.862+47_862+48delinsAG