Canonical Allele Identifier: CA368370622
Gene: CYP3A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768360A>C , CM000669.2:g.99768360A>C GRCh38
NC_000007.13:g.99365983A>C , CM000669.1:g.99365983A>C GRCh37
NC_000007.12:g.99203919A>C NCBI36
NG_008421.1:g.20826T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.664T>G ENSP00000337915.3:p.Ser222Ala
ENST00000651514.1:c.664T>G MANE Select ENSP00000498939.1:p.Ser222Ala
ENST00000651783.1:c.205T>G ENSP00000498924.1:p.Ser69Ala
ENST00000652018.1:c.517T>G ENSP00000498733.1:p.Ser173Ala
ENST00000336411.6:c.664T>G ENSP00000337915.2:p.Ser222Ala
ENST00000354593.6:c.214T>G ENSP00000346607.2:p.Ser72Ala
NM_001202855.2:c.664T>G NP_001189784.1:p.Ser222Ala
NM_017460.5:c.664T>G NP_059488.2:p.Ser222Ala
XM_011515841.1:c.664T>G XP_011514143.1:p.Ser222Ala
XM_011515842.1:c.664T>G XP_011514144.1:p.Ser222Ala
NM_017460.6:c.664T>G MANE Select NP_059488.2:p.Ser222Ala
NM_001202855.3:c.664T>G NP_001189784.1:p.Ser222Ala