Canonical Allele Identifier: CA368373365

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99367767A>G (hg19) ; chr7:g.99770144A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770144A>G , CM000669.2:g.99770144A>G	GRCh38
NC_000007.13:g.99367767A>G , CM000669.1:g.99367767A>G	GRCh37
NC_000007.12:g.99205703A>G	NCBI36
NG_008421.1:g.19042T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.410T>C	ENSP00000337915.3:p.Phe137Ser
ENST00000651514.1:c.410T>C MANE Select	ENSP00000498939.1:p.Phe137Ser
ENST00000651783.1:c.58-1637T>C	ENSP00000498924.1:n.58-1637T>C
ENST00000652018.1:c.263T>C	ENSP00000498733.1:p.Phe88Ser
ENST00000336411.6:c.410T>C	ENSP00000337915.2:p.Phe137Ser
ENST00000354593.6:c.72-1642T>C	ENSP00000346607.2:n.72-1642T>C
ENST00000415003.1:c.449T>C	ENSP00000397208.1:p.Phe150Ser
ENST00000480043.1:n.307T>C
NM_001202855.2:c.410T>C	NP_001189784.1:p.Phe137Ser
NM_017460.5:c.410T>C	NP_059488.2:p.Phe137Ser
XM_011515841.1:c.410T>C	XP_011514143.1:p.Phe137Ser
XM_011515842.1:c.410T>C	XP_011514144.1:p.Phe137Ser
NM_017460.6:c.410T>C MANE Select	NP_059488.2:p.Phe137Ser
NM_001202855.3:c.410T>C	NP_001189784.1:p.Phe137Ser