Canonical Allele Identifier: CA368370923
Gene: CYP3A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768415A>C , CM000669.2:g.99768415A>C GRCh38
NC_000007.13:g.99366038A>C , CM000669.1:g.99366038A>C GRCh37
NC_000007.12:g.99203974A>C NCBI36
NG_008421.1:g.20771T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.609T>G ENSP00000337915.3:p.Phe203Leu
ENST00000651514.1:c.609T>G MANE Select ENSP00000498939.1:p.Phe203Leu
ENST00000651783.1:c.150T>G ENSP00000498924.1:p.Phe50Leu
ENST00000652018.1:c.462T>G ENSP00000498733.1:p.Phe154Leu
ENST00000336411.6:c.609T>G ENSP00000337915.2:p.Phe203Leu
ENST00000354593.6:c.159T>G ENSP00000346607.2:p.Phe53Leu
NM_001202855.2:c.609T>G NP_001189784.1:p.Phe203Leu
NM_017460.5:c.609T>G NP_059488.2:p.Phe203Leu
XM_011515841.1:c.609T>G XP_011514143.1:p.Phe203Leu
XM_011515842.1:c.609T>G XP_011514144.1:p.Phe203Leu
NM_017460.6:c.609T>G MANE Select NP_059488.2:p.Phe203Leu
NM_001202855.3:c.609T>G NP_001189784.1:p.Phe203Leu