Canonical Allele Identifier: CA456690166

Gene: CYP3A4

Linked Data

• COSMIC: COSM1488832
• MyVariant Identifiers: chr7:g.99366074C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768451C>T , CM000669.2:g.99768451C>T	GRCh38
NC_000007.13:g.99366074C>T , CM000669.1:g.99366074C>T	GRCh37
NC_000007.12:g.99204010C>T	NCBI36
NG_008421.1:g.20735G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.573G>A	ENSP00000337915.3:p.Val191=
ENST00000651514.1:c.573G>A MANE Select	ENSP00000498939.1:p.Val191=
ENST00000651783.1:c.114G>A	ENSP00000498924.1:p.Val38=
ENST00000652018.1:c.426G>A	ENSP00000498733.1:p.Val142=
ENST00000336411.6:c.573G>A	ENSP00000337915.2:p.Val191=
ENST00000354593.6:c.123G>A	ENSP00000346607.2:p.Val41=
NM_001202855.2:c.573G>A	NP_001189784.1:p.Val191=
NM_017460.5:c.573G>A	NP_059488.2:p.Val191=
XM_011515841.1:c.573G>A	XP_011514143.1:p.Val191=
XM_011515842.1:c.573G>A	XP_011514144.1:p.Val191=
NM_017460.6:c.573G>A MANE Select	NP_059488.2:p.Val191=
NM_001202855.3:c.573G>A	NP_001189784.1:p.Val191=