Canonical Allele Identifier: CA163153417
Gene: CYP3A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768465T>A , CM000669.2:g.99768465T>A GRCh38
NC_000007.13:g.99366088T>A , CM000669.1:g.99366088T>A GRCh37
NC_000007.12:g.99204024T>A NCBI36
NG_008421.1:g.20721A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.559A>T ENSP00000337915.3:p.Thr187Ser
ENST00000651514.1:c.559A>T MANE Select ENSP00000498939.1:p.Thr187Ser
ENST00000651783.1:c.100A>T ENSP00000498924.1:p.Thr34Ser
ENST00000652018.1:c.412A>T ENSP00000498733.1:p.Thr138Ser
ENST00000336411.6:c.559A>T ENSP00000337915.2:p.Thr187Ser
ENST00000354593.6:c.109A>T ENSP00000346607.2:p.Thr37Ser
NM_001202855.2:c.559A>T NP_001189784.1:p.Thr187Ser
NM_017460.5:c.559A>T NP_059488.2:p.Thr187Ser
XM_011515841.1:c.559A>T XP_011514143.1:p.Thr187Ser
XM_011515842.1:c.559A>T XP_011514144.1:p.Thr187Ser
NM_017460.6:c.559A>T MANE Select NP_059488.2:p.Thr187Ser
NM_001202855.3:c.559A>T NP_001189784.1:p.Thr187Ser