Canonical Allele Identifier: CA368368605

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358528C>G (hg19) ; chr7:g.99760905C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760905C>G , CM000669.2:g.99760905C>G	GRCh38
NC_000007.13:g.99358528C>G , CM000669.1:g.99358528C>G	GRCh37
NC_000007.12:g.99196464C>G	NCBI36
NG_008421.1:g.28281G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1423G>C	ENSP00000337915.3:p.Gly475Arg
ENST00000651162.1:n.765G>C
ENST00000651514.1:c.1330G>C MANE Select	ENSP00000498939.1:p.Gly444Arg
ENST00000651783.1:c.871G>C	ENSP00000498924.1:p.Gly291Arg
ENST00000652018.1:c.1183G>C	ENSP00000498733.1:p.Gly395Arg
ENST00000336411.6:c.1330G>C	ENSP00000337915.2:p.Gly444Arg
ENST00000354593.6:c.880G>C	ENSP00000346607.2:p.Gly294Arg
NM_001202855.2:c.1327G>C	NP_001189784.1:p.Gly443Arg
NM_017460.5:c.1330G>C	NP_059488.2:p.Gly444Arg
XM_011515841.1:c.1423G>C	XP_011514143.1:p.Gly475Arg
XM_011515842.1:c.1420G>C	XP_011514144.1:p.Gly474Arg
NM_017460.6:c.1330G>C MANE Select	NP_059488.2:p.Gly444Arg
NM_001202855.3:c.1327G>C	NP_001189784.1:p.Gly443Arg