Canonical Allele Identifier: CA1729177792
Community Standard Title: NM_017460.6(CYP3A4):c.1026+608C=
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99763247G= , CM000669.2:g.99763247G= GRCh38
NC_000007.13:g.99360870G= , CM000669.1:g.99360870G= GRCh37
NC_000007.12:g.99198806G= NCBI36
NG_008421.1:g.25939C=

Transcript Alleles

HGVS Amino-acid Change
NM_017460.6:c.1026+608C= MANE Select NP_059488.2:n.1026+608C=
ENST00000651514.1:c.1026+608C= MANE Select ENSP00000498939.1:n.1026+608C=
NM_001202855.2:c.1023+608C= NP_001189784.1:n.1023+608C=
NM_001202855.3:c.1023+608C= NP_001189784.1:n.1023+608C=
NM_017460.5:c.1026+608C= NP_059488.2:n.1026+608C=
ENST00000336411.6:c.1026+608C= ENSP00000337915.2:n.1026+608C=
ENST00000336411.7:c.1026+608C= ENSP00000337915.3:n.1026+608C=
ENST00000354593.6:c.576+608C= ENSP00000346607.2:n.576+608C=
ENST00000651162.1:n.461+608C=
ENST00000651783.1:c.567+608C= ENSP00000498924.1:n.567+608C=
ENST00000652018.1:c.879+608C= ENSP00000498733.1:n.879+608C=
XM_011515841.1:c.1026+608C= XP_011514143.1:n.1026+608C=
XM_011515842.1:c.1023+608C= XP_011514144.1:n.1023+608C=