Canonical Allele Identifier: CA163151020

Gene: CYP3A4

Linked Data

• dbSNP Id: rs554707466
• MyVariant Identifiers: chr7:g.99358246_99358248del (hg19) ; chr7:g.99760623_99760625del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760626_99760628del , CM000669.2:g.99760626_99760628del	GRCh38
NC_000007.13:g.99358249_99358251del , CM000669.1:g.99358249_99358251del	GRCh37
NC_000007.12:g.99196185_99196187del	NCBI36
NG_008421.1:g.28561_28563del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1509+194_1509+196del	ENSP00000337915.3:n.1509+194_1509+196del
ENST00000651162.1:n.851+194_851+196del
ENST00000651514.1:c.1416+194_1416+196del MANE Select	ENSP00000498939.1:n.1416+194_1416+196del
ENST00000651783.1:c.957+194_957+196del	ENSP00000498924.1:n.957+194_957+196del
ENST00000652018.1:c.1269+194_1269+196del	ENSP00000498733.1:n.1269+194_1269+196del
ENST00000336411.6:c.1416+194_1416+196del	ENSP00000337915.2:n.1416+194_1416+196del
ENST00000354593.6:c.966+194_966+196del	ENSP00000346607.2:n.966+194_966+196del
NM_001202855.2:c.1413+194_1413+196del	NP_001189784.1:n.1413+194_1413+196del
NM_017460.5:c.1416+194_1416+196del	NP_059488.2:n.1416+194_1416+196del
XM_011515841.1:c.1509+194_1509+196del	XP_011514143.1:n.1509+194_1509+196del
XM_011515842.1:c.1506+194_1506+196del	XP_011514144.1:n.1506+194_1506+196del
NM_017460.6:c.1416+194_1416+196del MANE Select	NP_059488.2:n.1416+194_1416+196del
NM_001202855.3:c.1413+194_1413+196del	NP_001189784.1:n.1413+194_1413+196del