Canonical Allele Identifier: CA163151140

Gene: CYP3A4

Linked Data

• dbSNP Id: rs72552796
• COSMIC: COSM4675977
• MyVariant Identifiers: chr7:g.99358521C>T (hg19) ; chr7:g.99760898C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760898C>T , CM000669.2:g.99760898C>T	GRCh38
NC_000007.13:g.99358521C>T , CM000669.1:g.99358521C>T	GRCh37
NC_000007.12:g.99196457C>T	NCBI36
NG_008421.1:g.28288G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1430G>A	ENSP00000337915.3:p.Arg477Lys
ENST00000651162.1:n.772G>A
ENST00000651514.1:c.1337G>A MANE Select	ENSP00000498939.1:p.Arg446Lys
ENST00000651783.1:c.878G>A	ENSP00000498924.1:p.Arg293Lys
ENST00000652018.1:c.1190G>A	ENSP00000498733.1:p.Arg397Lys
ENST00000336411.6:c.1337G>A	ENSP00000337915.2:p.Arg446Lys
ENST00000354593.6:c.887G>A	ENSP00000346607.2:p.Arg296Lys
NM_001202855.2:c.1334G>A	NP_001189784.1:p.Arg445Lys
NM_017460.5:c.1337G>A	NP_059488.2:p.Arg446Lys
XM_011515841.1:c.1430G>A	XP_011514143.1:p.Arg477Lys
XM_011515842.1:c.1427G>A	XP_011514144.1:p.Arg476Lys
NM_017460.6:c.1337G>A MANE Select	NP_059488.2:p.Arg446Lys
NM_001202855.3:c.1334G>A	NP_001189784.1:p.Arg445Lys