Canonical Allele Identifier: CA16309262

Gene: CYP3A4

Linked Data

• dbSNP Id: rs71581998
• MyVariant Identifiers: chr7:g.99359841A>G (hg19) ; chr7:g.99762218A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762218A>G , CM000669.2:g.99762218A>G	GRCh38
NC_000007.13:g.99359841A>G , CM000669.1:g.99359841A>G	GRCh37
NC_000007.12:g.99197777A>G	NCBI36
NG_008421.1:g.26968T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1076T>C	ENSP00000337915.3:p.Val359Ala
ENST00000651162.1:n.511T>C
ENST00000651514.1:c.1076T>C MANE Select	ENSP00000498939.1:p.Val359Ala
ENST00000651783.1:c.617T>C	ENSP00000498924.1:p.Val206Ala
ENST00000652018.1:c.929T>C	ENSP00000498733.1:p.Val310Ala
ENST00000336411.6:c.1076T>C	ENSP00000337915.2:p.Val359Ala
ENST00000354593.6:c.626T>C	ENSP00000346607.2:p.Val209Ala
NM_001202855.2:c.1073T>C	NP_001189784.1:p.Val358Ala
NM_017460.5:c.1076T>C	NP_059488.2:p.Val359Ala
XM_011515841.1:c.1076T>C	XP_011514143.1:p.Val359Ala
XM_011515842.1:c.1073T>C	XP_011514144.1:p.Val358Ala
NM_017460.6:c.1076T>C MANE Select	NP_059488.2:p.Val359Ala
NM_001202855.3:c.1073T>C	NP_001189784.1:p.Val358Ala