Canonical Allele Identifier: CA368368747
Gene: CYP3A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99760968T>C , CM000669.2:g.99760968T>C GRCh38
NC_000007.13:g.99358591T>C , CM000669.1:g.99358591T>C GRCh37
NC_000007.12:g.99196527T>C NCBI36
NG_008421.1:g.28218A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.1360A>G ENSP00000337915.3:p.Asn454Asp
ENST00000651162.1:n.702A>G
ENST00000651514.1:c.1267A>G MANE Select ENSP00000498939.1:p.Asn423Asp
ENST00000651783.1:c.808A>G ENSP00000498924.1:p.Asn270Asp
ENST00000652018.1:c.1120A>G ENSP00000498733.1:p.Asn374Asp
ENST00000336411.6:c.1267A>G ENSP00000337915.2:p.Asn423Asp
ENST00000354593.6:c.817A>G ENSP00000346607.2:p.Asn273Asp
NM_001202855.2:c.1264A>G NP_001189784.1:p.Asn422Asp
NM_017460.5:c.1267A>G NP_059488.2:p.Asn423Asp
XM_011515841.1:c.1360A>G XP_011514143.1:p.Asn454Asp
XM_011515842.1:c.1357A>G XP_011514144.1:p.Asn453Asp
NM_017460.6:c.1267A>G MANE Select NP_059488.2:p.Asn423Asp
NM_001202855.3:c.1264A>G NP_001189784.1:p.Asn422Asp