Canonical Allele Identifier: CA1729180942
Community Standard Title: NM_017460.6(CYP3A4):c.577A= (p.Ile193=)
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768447T= , CM000669.2:g.99768447T= GRCh38
NC_000007.13:g.99366070T= , CM000669.1:g.99366070T= GRCh37
NC_000007.12:g.99204006T= NCBI36
NG_008421.1:g.20739A=

Transcript Alleles

HGVS Amino-acid Change
NM_017460.6:c.577A= MANE Select NP_059488.2:p.Ile193=
ENST00000651514.1:c.577A= MANE Select ENSP00000498939.1:p.Ile193=
NM_001202855.2:c.577A= NP_001189784.1:p.Ile193=
NM_001202855.3:c.577A= NP_001189784.1:p.Ile193=
NM_017460.5:c.577A= NP_059488.2:p.Ile193=
ENST00000336411.6:c.577A= ENSP00000337915.2:p.Ile193=
ENST00000336411.7:c.577A= ENSP00000337915.3:p.Ile193=
ENST00000354593.6:c.127A= ENSP00000346607.2:p.Ile43=
ENST00000651783.1:c.118A= ENSP00000498924.1:p.Ile40=
ENST00000652018.1:c.430A= ENSP00000498733.1:p.Ile144=
XM_011515841.1:c.577A= XP_011514143.1:p.Ile193=
XM_011515842.1:c.577A= XP_011514144.1:p.Ile193=