Canonical Allele Identifier: CA1729176796
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99760963C= , CM000669.2:g.99760963C= GRCh38
NC_000007.13:g.99358586C= , CM000669.1:g.99358586C= GRCh37
NC_000007.12:g.99196522C= NCBI36
NG_008421.1:g.28223G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.1365G= ENSP00000337915.3:p.Lys455=
ENST00000651162.1:n.707G=
ENST00000651514.1:c.1272G= MANE Select ENSP00000498939.1:p.Lys424=
ENST00000651783.1:c.813G= ENSP00000498924.1:p.Lys271=
ENST00000652018.1:c.1125G= ENSP00000498733.1:p.Lys375=
ENST00000336411.6:c.1272G= ENSP00000337915.2:p.Lys424=
ENST00000354593.6:c.822G= ENSP00000346607.2:p.Lys274=
NM_001202855.2:c.1269G= NP_001189784.1:p.Lys423=
NM_017460.5:c.1272G= NP_059488.2:p.Lys424=
XM_011515841.1:c.1365G= XP_011514143.1:p.Lys455=
XM_011515842.1:c.1362G= XP_011514144.1:p.Lys454=
NM_017460.6:c.1272G= MANE Select NP_059488.2:p.Lys424=
NM_001202855.3:c.1269G= NP_001189784.1:p.Lys423=