Canonical Allele Identifier: CA368367698

Gene: CYP3A4

Linked Data

• gnomAD v4: 7-99760865-A-T
• MyVariant Identifiers: chr7:g.99358488A>T (hg19) ; chr7:g.99760865A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760865A>T , CM000669.2:g.99760865A>T	GRCh38
NC_000007.13:g.99358488A>T , CM000669.1:g.99358488A>T	GRCh37
NC_000007.12:g.99196424A>T	NCBI36
NG_008421.1:g.28321T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1463T>A	ENSP00000337915.3:p.Ile488Asn
ENST00000651162.1:n.805T>A
ENST00000651514.1:c.1370T>A MANE Select	ENSP00000498939.1:p.Ile457Asn
ENST00000651783.1:c.911T>A	ENSP00000498924.1:p.Ile304Asn
ENST00000652018.1:c.1223T>A	ENSP00000498733.1:p.Ile408Asn
ENST00000336411.6:c.1370T>A	ENSP00000337915.2:p.Ile457Asn
ENST00000354593.6:c.920T>A	ENSP00000346607.2:p.Ile307Asn
NM_001202855.2:c.1367T>A	NP_001189784.1:p.Ile456Asn
NM_017460.5:c.1370T>A	NP_059488.2:p.Ile457Asn
XM_011515841.1:c.1463T>A	XP_011514143.1:p.Ile488Asn
XM_011515842.1:c.1460T>A	XP_011514144.1:p.Ile487Asn
NM_017460.6:c.1370T>A MANE Select	NP_059488.2:p.Ile457Asn
NM_001202855.3:c.1367T>A	NP_001189784.1:p.Ile456Asn