Canonical Allele Identifier: CA368367537

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99760827-C-G
• MyVariant Identifiers: chr7:g.99358450C>G (hg19) ; chr7:g.99760827C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760827C>G , CM000669.2:g.99760827C>G	GRCh38
NC_000007.13:g.99358450C>G , CM000669.1:g.99358450C>G	GRCh37
NC_000007.12:g.99196386C>G	NCBI36
NG_008421.1:g.28359G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1501G>C	ENSP00000337915.3:p.Glu501Gln
ENST00000651162.1:n.843G>C
ENST00000651514.1:c.1408G>C MANE Select	ENSP00000498939.1:p.Glu470Gln
ENST00000651783.1:c.949G>C	ENSP00000498924.1:p.Glu317Gln
ENST00000652018.1:c.1261G>C	ENSP00000498733.1:p.Glu421Gln
ENST00000336411.6:c.1408G>C	ENSP00000337915.2:p.Glu470Gln
ENST00000354593.6:c.958G>C	ENSP00000346607.2:p.Glu320Gln
NM_001202855.2:c.1405G>C	NP_001189784.1:p.Glu469Gln
NM_017460.5:c.1408G>C	NP_059488.2:p.Glu470Gln
XM_011515841.1:c.1501G>C	XP_011514143.1:p.Glu501Gln
XM_011515842.1:c.1498G>C	XP_011514144.1:p.Glu500Gln
NM_017460.6:c.1408G>C MANE Select	NP_059488.2:p.Glu470Gln
NM_001202855.3:c.1405G>C	NP_001189784.1:p.Glu469Gln