Canonical Allele Identifier: CA456686443

Gene: CYP3A4

Linked Data

• dbSNP Id: rs2151553348
• gnomAD v4: 7-99760843-G-A
• MyVariant Identifiers: chr7:g.99358466G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760843G>A , CM000669.2:g.99760843G>A	GRCh38
NC_000007.13:g.99358466G>A , CM000669.1:g.99358466G>A	GRCh37
NC_000007.12:g.99196402G>A	NCBI36
NG_008421.1:g.28343C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1485C>T	ENSP00000337915.3:p.Ser495=
ENST00000651162.1:n.827C>T
ENST00000651514.1:c.1392C>T MANE Select	ENSP00000498939.1:p.Ser464=
ENST00000651783.1:c.933C>T	ENSP00000498924.1:p.Ser311=
ENST00000652018.1:c.1245C>T	ENSP00000498733.1:p.Ser415=
ENST00000336411.6:c.1392C>T	ENSP00000337915.2:p.Ser464=
ENST00000354593.6:c.942C>T	ENSP00000346607.2:p.Ser314=
NM_001202855.2:c.1389C>T	NP_001189784.1:p.Ser463=
NM_017460.5:c.1392C>T	NP_059488.2:p.Ser464=
XM_011515841.1:c.1485C>T	XP_011514143.1:p.Ser495=
XM_011515842.1:c.1482C>T	XP_011514144.1:p.Ser494=
NM_017460.6:c.1392C>T MANE Select	NP_059488.2:p.Ser464=
NM_001202855.3:c.1389C>T	NP_001189784.1:p.Ser463=