Canonical Allele Identifier: CA1729175807
Community Standard Title: NM_017460.6(CYP3A4):c.1417-124A=
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99758352T= , CM000669.2:g.99758352T= GRCh38
NC_000007.13:g.99355975T= , CM000669.1:g.99355975T= GRCh37
NC_000007.12:g.99193911T= NCBI36
NG_008421.1:g.30834A=

Transcript Alleles

HGVS Amino-acid Change
NM_017460.6:c.1417-124A= MANE Select NP_059488.2:n.1417-124A=
ENST00000651514.1:c.1417-124A= MANE Select ENSP00000498939.1:n.1417-124A=
NM_001202855.2:c.1414-124A= NP_001189784.1:n.1414-124A=
NM_001202855.3:c.1414-124A= NP_001189784.1:n.1414-124A=
NM_017460.5:c.1417-124A= NP_059488.2:n.1417-124A=
ENST00000336411.6:c.1417-124A= ENSP00000337915.2:n.1417-124A=
ENST00000336411.7:c.1510-124A= ENSP00000337915.3:n.1510-124A=
ENST00000354593.6:c.967-124A= ENSP00000346607.2:n.967-124A=
ENST00000651162.1:n.852-124A=
ENST00000651783.1:c.958-124A= ENSP00000498924.1:n.958-124A=
ENST00000652018.1:c.1270-124A= ENSP00000498733.1:n.1270-124A=
XM_011515841.1:c.1510-124A= XP_011514143.1:n.1510-124A=
XM_011515842.1:c.1507-124A= XP_011514144.1:n.1507-124A=