Canonical Allele Identifier: CA456690120

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99365993T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768370T>C , CM000669.2:g.99768370T>C	GRCh38
NC_000007.13:g.99365993T>C , CM000669.1:g.99365993T>C	GRCh37
NC_000007.12:g.99203929T>C	NCBI36
NG_008421.1:g.20816A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.654A>G	ENSP00000337915.3:p.Pro218=
ENST00000651514.1:c.654A>G MANE Select	ENSP00000498939.1:p.Pro218=
ENST00000651783.1:c.195A>G	ENSP00000498924.1:p.Pro65=
ENST00000652018.1:c.507A>G	ENSP00000498733.1:p.Pro169=
ENST00000336411.6:c.654A>G	ENSP00000337915.2:p.Pro218=
ENST00000354593.6:c.204A>G	ENSP00000346607.2:p.Pro68=
NM_001202855.2:c.654A>G	NP_001189784.1:p.Pro218=
NM_017460.5:c.654A>G	NP_059488.2:p.Pro218=
XM_011515841.1:c.654A>G	XP_011514143.1:p.Pro218=
XM_011515842.1:c.654A>G	XP_011514144.1:p.Pro218=
NM_017460.6:c.654A>G MANE Select	NP_059488.2:p.Pro218=
NM_001202855.3:c.654A>G	NP_001189784.1:p.Pro218=