Canonical Allele Identifier: CA368368825
Gene: CYP3A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99762056T>A , CM000669.2:g.99762056T>A GRCh38
NC_000007.13:g.99359679T>A , CM000669.1:g.99359679T>A GRCh37
NC_000007.12:g.99197615T>A NCBI36
NG_008421.1:g.27130A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.1238A>T ENSP00000337915.3:p.Lys413Met
ENST00000651162.1:n.673A>T
ENST00000651514.1:c.1238A>T MANE Select ENSP00000498939.1:p.Lys413Met
ENST00000651783.1:c.779A>T ENSP00000498924.1:p.Lys260Met
ENST00000652018.1:c.1091A>T ENSP00000498733.1:p.Lys364Met
ENST00000336411.6:c.1238A>T ENSP00000337915.2:p.Lys413Met
ENST00000354593.6:c.788A>T ENSP00000346607.2:p.Lys263Met
NM_001202855.2:c.1235A>T NP_001189784.1:p.Lys412Met
NM_017460.5:c.1238A>T NP_059488.2:p.Lys413Met
XM_011515841.1:c.1238A>T XP_011514143.1:p.Lys413Met
XM_011515842.1:c.1235A>T XP_011514144.1:p.Lys412Met
NM_017460.6:c.1238A>T MANE Select NP_059488.2:p.Lys413Met
NM_001202855.3:c.1235A>T NP_001189784.1:p.Lys412Met