Canonical Allele Identifier: CA456686463

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99760863-T-G
• MyVariant Identifiers: chr7:g.99358486T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760863T>G , CM000669.2:g.99760863T>G	GRCh38
NC_000007.13:g.99358486T>G , CM000669.1:g.99358486T>G	GRCh37
NC_000007.12:g.99196422T>G	NCBI36
NG_008421.1:g.28323A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1465A>C	ENSP00000337915.3:p.Arg489=
ENST00000651162.1:n.807A>C
ENST00000651514.1:c.1372A>C MANE Select	ENSP00000498939.1:p.Arg458=
ENST00000651783.1:c.913A>C	ENSP00000498924.1:p.Arg305=
ENST00000652018.1:c.1225A>C	ENSP00000498733.1:p.Arg409=
ENST00000336411.6:c.1372A>C	ENSP00000337915.2:p.Arg458=
ENST00000354593.6:c.922A>C	ENSP00000346607.2:p.Arg308=
NM_001202855.2:c.1369A>C	NP_001189784.1:p.Arg457=
NM_017460.5:c.1372A>C	NP_059488.2:p.Arg458=
XM_011515841.1:c.1465A>C	XP_011514143.1:p.Arg489=
XM_011515842.1:c.1462A>C	XP_011514144.1:p.Arg488=
NM_017460.6:c.1372A>C MANE Select	NP_059488.2:p.Arg458=
NM_001202855.3:c.1369A>C	NP_001189784.1:p.Arg457=