Canonical Allele Identifier: CA368371228

Gene: CYP3A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768471T>A , CM000669.2:g.99768471T>A	GRCh38
NC_000007.13:g.99366094T>A , CM000669.1:g.99366094T>A	GRCh37
NC_000007.12:g.99204030T>A	NCBI36
NG_008421.1:g.20715A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.553A>T	ENSP00000337915.3:p.Thr185Ser
ENST00000651514.1:c.553A>T MANE Select	ENSP00000498939.1:p.Thr185Ser
ENST00000651783.1:c.94A>T	ENSP00000498924.1:p.Thr32Ser
ENST00000652018.1:c.406A>T	ENSP00000498733.1:p.Thr136Ser
ENST00000336411.6:c.553A>T	ENSP00000337915.2:p.Thr185Ser
ENST00000354593.6:c.103A>T	ENSP00000346607.2:p.Thr35Ser
NM_001202855.2:c.553A>T	NP_001189784.1:p.Thr185Ser
NM_017460.5:c.553A>T	NP_059488.2:p.Thr185Ser
XM_011515841.1:c.553A>T	XP_011514143.1:p.Thr185Ser
XM_011515842.1:c.553A>T	XP_011514144.1:p.Thr185Ser
NM_017460.6:c.553A>T MANE Select	NP_059488.2:p.Thr185Ser
NM_001202855.3:c.553A>T	NP_001189784.1:p.Thr185Ser