Canonical Allele Identifier: CA368367657

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358477G>C (hg19) ; chr7:g.99760854G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760854G>C , CM000669.2:g.99760854G>C	GRCh38
NC_000007.13:g.99358477G>C , CM000669.1:g.99358477G>C	GRCh37
NC_000007.12:g.99196413G>C	NCBI36
NG_008421.1:g.28332C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1474C>G	ENSP00000337915.3:p.Gln492Glu
ENST00000651162.1:n.816C>G
ENST00000651514.1:c.1381C>G MANE Select	ENSP00000498939.1:p.Gln461Glu
ENST00000651783.1:c.922C>G	ENSP00000498924.1:p.Gln308Glu
ENST00000652018.1:c.1234C>G	ENSP00000498733.1:p.Gln412Glu
ENST00000336411.6:c.1381C>G	ENSP00000337915.2:p.Gln461Glu
ENST00000354593.6:c.931C>G	ENSP00000346607.2:p.Gln311Glu
NM_001202855.2:c.1378C>G	NP_001189784.1:p.Gln460Glu
NM_017460.5:c.1381C>G	NP_059488.2:p.Gln461Glu
XM_011515841.1:c.1474C>G	XP_011514143.1:p.Gln492Glu
XM_011515842.1:c.1471C>G	XP_011514144.1:p.Gln491Glu
NM_017460.6:c.1381C>G MANE Select	NP_059488.2:p.Gln461Glu
NM_001202855.3:c.1378C>G	NP_001189784.1:p.Gln460Glu